Products

Product Name: Insulin Lispro Injection 100 Units/mL (U-100) – Prefilled KwikPen Active Ingredient: Insulin Lispro Dosage Form: Injectable solution Strength: 100 Units/mL Presentation: 3 mL prefilled pen Category: Diabetes / Antidiabetic / Insulin Insulin Lispro is a rapid-acting insulin analogue used to improve blood-glucose control in people with diabetes who require insulin therapy. Official prescribing information describes U-100 insulin lispro as a rapid-acting insulin and provides administration and storage requirements. Product Overview Insulin Lispro 100 Units/mL is supplied in a prefilled pen presentation designed for subcutaneous insulin administration. The U-100 KwikPen presentation contains 3 mL (300 units) of insulin lispro. The product shown in the supplied image is a Humalog/insulin lispro KwikPen-style presentation. Product branding, packaging, registration status and availability can differ between countries. Uses of Insulin Lispro Insulin lispro may be prescribed for: Diabetes mellitus requiring insulin therapy Improvement of blood-glucose control Mealtime insulin management as part of an individualized diabetes treatment plan The exact dose and timing should be determined by the treating healthcare professional based on the patient's glucose levels, diet, insulin regimen and other clinical factors. Important Safety Considerations Insulin can cause hypoglycemia (low blood glucose) if the amount administered is greater than required. Patients should follow their prescribed insulin regimen and glucose-monitoring instructions. The KwikPen should not be shared between patients, even when the needle is changed. Insulin storage is also important. Unopened U-100 insulin lispro is generally refrigerated at 2°C–8°C (36°F–46°F) and should not be frozen, subject to the specific product's approved labeling. International Medicine Trading & Export Insulin products are temperature-sensitive pharmaceutical products, so international trading requires appropriate packaging, storage and transportation procedures. Import requirements, prescription rules, product registration, cold-chain requirements and customs documentation vary by destination. Target export markets: 🇺🇸 USA 🇬🇧 UK 🇸🇬 Singapore 🇹🇭 Thailand 🇦🇪 UAE 🇦🇺 Australia 🇲🇾 Malaysia 🇳🇿 New Zealand 🌍 Other international destinations, subject to applicable regulations For international orders, buyers should verify the medicine's legality, registration/import requirements and prescription requirements in their destination country before placing an order. Trading FAQs 1. What is Insulin Lispro? Insulin lispro is a rapid-acting insulin analogue used for blood-glucose management in patients requiring insulin therapy. 2. What strength is this product? The product shown is Insulin Lispro 100 Units/mL (U-100). 3. What is the KwikPen volume? The U-100 KwikPen presentation is a 3 mL prefilled pen containing 300 units. 4. Is Insulin Lispro prescription medicine? Yes. Insulin therapy should be used according to a healthcare professional's prescription and instructions. 5. Can the pen be shared? No. A KwikPen is intended for use by a single patient and should never be shared. 6. How should insulin be shipped internationally? Because insulin is temperature-sensitive, appropriate temperature-controlled handling and packaging should be arranged according to the manufacturer's requirements and applicable transport regulations. 7. Can you export Insulin Lispro worldwide? Availability depends on the destination country's pharmaceutical import, prescription, registration and customs requirements. Orders should be evaluated according to the regulations applicable to the destination. 8. Do you provide international medicine supply? MEDINDIA EXPORT / BizHQ can assist with international pharmaceutical supply inquiries, subject to product availability and destination-country regulations. Why Contact MEDINDIA EXPORT? We provide pharmaceutical export and international medicine supply assistance for customers and trading partners across multiple international markets. 🌐 Website: www.medicineindiaexport.com 📧 Email: sales.medindiaexport@gmail.com 📱 WhatsApp: +91 7218129896

Product Name: Caverject Impulse 20 mcg Active Ingredient: Alprostadil Strength: 20 mcg Dosage Form: Injection Therapeutic Category: Erectile Dysfunction / Urology Manufacturer/Brand: Pfizer Prescription Status: Prescription medicine Product Overview Caverject Impulse 20 mcg contains Alprostadil, a prostaglandin medicine used under medical supervision for the treatment of erectile dysfunction. The product should be prescribed and administered according to the manufacturer's instructions and applicable local regulations. Key Product Information Composition: Alprostadil 20 mcg Product Type: Pharmaceutical injection Therapeutic Area: Urology Indication: Erectile dysfunction Route: Intracavernosal administration as directed by a healthcare professional Packaging: As supplied by the manufacturer Storage: Follow the manufacturer's approved storage conditions Availability: Subject to stock and applicable export/import regulations Uses Caverject Impulse 20 mcg may be prescribed for the management of erectile dysfunction. The appropriate dose and administration technique must be determined by a qualified healthcare professional. Important Safety Information This is a prescription medicine. Patients should: Use it only under appropriate medical supervision. Follow the prescribed dosage and administration instructions. Not change the dose without consulting their healthcare professional. Seek urgent medical attention for a prolonged or painful erection. Follow the official product leaflet for contraindications, warnings and adverse effects. International Export Destinations We accept pharmaceutical sourcing and export inquiries for: USA | UK | Singapore | Thailand | UAE | Australia | Malaysia | New Zealand International orders are subject to product availability, prescription requirements, import permissions, customs procedures and pharmaceutical regulations applicable in the destination country. Trading & Export FAQs Q: Is Caverject Impulse 20 mcg available for export? A: Availability depends on current stock and the regulatory requirements of the destination market. Q: What is the active ingredient? A: The active ingredient is Alprostadil 20 mcg. Q: Is a prescription required? A: Caverject Impulse is a prescription medicine. Requirements vary by country. Q: Can I request a quotation? A: Yes. Contact our export team with the required quantity and destination country. Q: Do you provide international shipping? A: International shipping can be arranged where legally permitted and subject to applicable import and export requirements. Request a Quote For Caverject Impulse 20 mcg availability, pricing, quantity and export information, contact: 🌐 Website: www.medicineindiaexport.com 📧 Email: sales.medindiaexport@gmail.com 📱 WhatsApp: +91 7218129896 MEDINDIA EXPORT – International Pharmaceutical Export & Sourcing

Product: Aqualyx Fat-Dissolving Injections Dosage/Form: Injectable Solution Application: Professional Aesthetic Use Supply: International B2B Pharmaceutical Export Product Overview Aqualyx Fat-Dissolving Injections are associated with professional aesthetic procedures involving localized subcutaneous fat reduction. The product should be handled and administered only by appropriately qualified healthcare professionals and in accordance with the applicable product information and regulations. At MEDINDIA EXPORT, we support international B2B buyers seeking pharmaceutical and healthcare-product sourcing from India, subject to product availability and destination-country requirements. Key Catalogue Information Product Name: Aqualyx Product Type: Fat-dissolving injectable Category: Aesthetic / Dermatology Dosage Form: Injectable Intended Setting: Professional healthcare/aesthetic practice Packaging: Subject to available manufacturer presentation Storage: According to current manufacturer instructions Export Availability: Subject to applicable regulations International Export Markets We accept B2B inquiries from international markets including the USA, UK, Singapore, Thailand, UAE, Australia, Malaysia, New Zealand, Canada, Germany, France, Italy, Spain, Netherlands, Belgium, Sweden, Norway, Denmark, Finland, Ireland, Switzerland, Austria, Poland, Portugal, Greece and other destinations, subject to applicable import regulations. Important Regulatory Information Regulatory approval, classification, permitted indications, import requirements, and availability of Aqualyx may differ between countries. Buyers should verify the product's current regulatory status and import requirements with the relevant authorities before placing an order. Injectable aesthetic products should not be purchased for self-administration. Use should be limited to appropriately qualified professionals who are legally authorized to perform the relevant procedure. B2B Export & Trading FAQs Q1. What category does Aqualyx belong to? Aqualyx is generally associated with aesthetic medicine, dermatology, cosmetic injectables, and localized body-contouring procedures. Q2. Is Aqualyx available for international export? Availability depends on the destination country, applicable export controls, product documentation, and import regulations. Q3. Can I request a bulk quotation? Yes. International B2B buyers can contact us with the required quantity and destination country for availability and quotation information. Q4. Do import requirements vary by country? Yes. Product registration, import authorization, documentation, customs requirements, and permitted use can differ significantly between jurisdictions. Q5. Can you provide product documentation? Available documentation can be discussed according to the specific product presentation, supplier documentation, and destination-country requirements. Q6. How can I place an international inquiry? Send the product name, required quantity, destination country, and any documentation requirements to our sales team. Contact MEDINDIA EXPORT 🌐 Website: www.medicineindiaexport.com 📧 Email: sales.medindiaexport@gmail.com 📱 WhatsApp: +91 7218129896 MEDINDIA EXPORT International Pharmaceutical Sourcing & Export

Product Category: Pharmaceutical / Injectable Preparation Product Name: Bacteriostatic Water for Injection USP Pack Size: 30 mL Dosage Form: Sterile Solution for Injection Standard: USP Product Overview Bacteriostatic Water for Injection USP 30 mL is a sterile preparation intended for use as a diluent or solvent for compatible injectable medications when specified by the product manufacturer or healthcare professional. It contains a bacteriostatic preservative and is supplied in a multidose container. Uses Bacteriostatic Water for Injection may be used for reconstituting or diluting compatible injectable medicines according to their approved product information and healthcare-professional instructions. Important Considerations Use only with medicines specifically compatible with bacteriostatic water. Follow the instructions supplied with the medication being reconstituted. Intended for professional medical use. Do not use if the container is damaged, leaking, or shows visible contamination. Storage and handling should follow the manufacturer's labelled instructions. Availability, importation, and use are subject to the regulations of the destination country. Trading & Export Availability MEDINDIA EXPORT supplies pharmaceutical products for international trade, subject to applicable export and destination-country regulations. Target Markets: USA, UK, Singapore, Thailand, Malaysia, Australia, New Zealand, UAE, Canada, Germany, France, Italy, Spain, Netherlands, Sweden, and other international destinations. Trading FAQs Q1. What is Bacteriostatic Water for Injection USP 30 mL? It is a sterile water-based preparation used as a diluent for compatible injectable medicines when specified by the medication's instructions. Q2. What is the pack size? The listed pack size is 30 mL. Q3. Can it be used with every injectable medicine? No. Compatibility depends on the specific medication. Always follow the manufacturer's approved instructions or advice from a qualified healthcare professional. Q4. Can you supply internationally? International supply may be available depending on destination-country regulations, documentation, and import requirements. Q5. How can I request a quotation? Contact MEDINDIA EXPORT with the required quantity, destination country, and product requirements. Why Contact MEDINDIA EXPORT? Pharmaceutical export support International sourcing assistance Product and quotation inquiries Support for documentation and shipping requirements Worldwide destination coverage subject to applicable regulations Product Inquiry For availability, pricing, packaging, and export requirements, contact us: 🌐 Website: www.medicineindiaexport.com 📧 Email: sales.medindiaexport@gmail.com 📱 WhatsApp: +91 7218129896

Anavar Max 10 mg contains oxandrolone 10 mg, an anabolic-androgenic steroid that is used medically in specific circumstances under the supervision of a qualified healthcare professional. Availability, prescribing requirements, import rules, and controlled-substance regulations differ significantly between countries. Product Overview Product Name: Anavar Max 10 mg Active Ingredient: Oxandrolone Strength: 10 mg Dosage Form: Tablet Category: Prescription Anabolic-Androgenic Steroid Therapeutic Use: Specific medically indicated conditions under professional supervision Supply: Subject to applicable prescription, pharmaceutical export, import, and regulatory requirements Uses of Oxandrolone Oxandrolone may be prescribed for certain medical conditions where an anabolic agent is considered appropriate. The exact indication and treatment protocol should be determined by a licensed healthcare professional. It should not be used for bodybuilding, athletic performance enhancement, or weight-loss purposes without appropriate medical supervision. Important Safety Information Oxandrolone can cause adverse effects and may interact with other medicines. Potential concerns include changes in liver function, lipid levels, hormonal effects, and other androgenic or anabolic effects. Patients should follow the prescribing physician's instructions and undergo appropriate monitoring where recommended. Pregnant individuals should not use androgenic anabolic steroids because of the potential for fetal harm. International Pharmaceutical Trading MEDINDIA EXPORT provides pharmaceutical sourcing and export support subject to applicable laws and regulatory requirements. International transactions involving prescription or controlled medicines may require documentation such as prescriptions, import permits, product registration, or authorization from the relevant regulatory authority. Countries & Markets Covered United States: California, Texas, Florida, New York, Illinois, Pennsylvania, Ohio, Georgia, North Carolina, New Jersey, Virginia, Washington, Arizona, Massachusetts and Michigan. United Kingdom: Greater London, Manchester, Birmingham, Liverpool, Sheffield, Bristol, Nottingham, Leicester, Southampton, Glasgow, Edinburgh, Cardiff and Belfast. Singapore: Central Region, Marina Bay, CBD, Jurong East, Woodlands, Queenstown, Tampines, Bedok, Orchard and Novena. Thailand: Bangkok, Chiang Mai, Phuket, Rayong, Chonburi, Nonthaburi, Samut Prakan, Pathum Thani, Khon Kaen and Udon Thani. Malaysia: Kuala Lumpur, Selangor, Johor, Penang, Sarawak, Putrajaya, Johor Bahru, Petaling Jaya and George Town. Australia: New South Wales, Victoria, Queensland, Western Australia, Sydney, Melbourne, Brisbane, Perth and Adelaide. United Arab Emirates, New Zealand and other international destinations: Availability and shipment are subject to destination-country pharmaceutical regulations, licensing requirements and customs clearance. Trading FAQs 1. What is Anavar Max 10 mg? Anavar Max 10 mg is a tablet containing oxandrolone, a prescription anabolic-androgenic steroid used for specific medical indications. 2. Is Anavar Max 10 mg a prescription medicine? Yes. Oxandrolone is a prescription medicine, and additional controlled-substance or import requirements may apply depending on the destination country. 3. Can oxandrolone be imported internationally? International importation depends on the laws of both the exporting and importing countries. Required permits, prescriptions, registrations or other documentation may apply. 4. Can it be supplied for bodybuilding? MEDINDIA EXPORT does not recommend or promote prescription medicines for non-medical performance enhancement. Supply should be for lawful and medically appropriate purposes. 5. Are the same regulations applicable in every country? No. Pharmaceutical and controlled-substance regulations differ between jurisdictions. Buyers and importers should verify requirements with their country's relevant health and customs authorities. 6. Is a prescription required? Requirements vary by jurisdiction, but oxandrolone is a prescription medicine and buyers should have appropriate medical documentation where required. 7. Can international buyers place an inquiry? International buyers may contact MEDINDIA EXPORT for product and regulatory information. Any transaction is subject to applicable export, import, prescription and regulatory requirements. 8. How should Anavar Max 10 mg be stored? Follow the storage instructions printed on the manufacturer's packaging and product documentation. Responsible Pharmaceutical Supply For prescription medicines such as oxandrolone, responsible international trading requires verification of the product, applicable documentation, destination-country requirements and lawful customs procedures before shipment. For product availability, documentation and compliant international trade inquiries: 🌐 Website: www.medicineindiaexport.com

Product Name: Semaglutide Injection 1 mg Active Ingredient: Semaglutide Strength: 1 mg Dosage Form: Injection Route: Subcutaneous Therapeutic Category: Diabetes / Weight Management / GLP-1 Receptor Agonist Prescription Status: Prescription medicine Product Overview Semaglutide is a long-acting GLP-1 receptor agonist. Depending on the specific branded product and country approval, semaglutide is used for type 2 diabetes management and/or chronic weight management. Uses Type 2 diabetes management with appropriately approved semaglutide products Weight management with appropriately approved products Helps regulate appetite and food intake as part of an approved treatment plan Key Benefits Once-weekly administration for products with a weekly dosing schedule Supports blood-glucose management in type 2 diabetes May support weight reduction when prescribed for chronic weight management Important Considerations Semaglutide should be used only according to the prescribing information for the specific product. Possible adverse effects include nausea, vomiting, diarrhea, constipation and abdominal discomfort. Important warnings and contraindications vary by product and country. Storage Storage requirements depend on the manufacturer and specific presentation. Maintain the required cold-chain conditions and follow the manufacturer's approved storage instructions. Trading FAQs 1. What is Semaglutide Injection 1 mg? It is an injectable semaglutide formulation containing 1 mg of semaglutide, used in certain approved treatment regimens. 2. What category does Semaglutide 1 mg belong to? It belongs primarily to the GLP-1 receptor agonist category and may be listed under Diabetes or Weight Management, depending on the product's approved indication. 3. Is Semaglutide 1 mg prescription-only? Yes. Semaglutide injections require appropriate medical supervision and prescription requirements vary by country. 4. Can Semaglutide 1 mg be exported internationally? International pharmaceutical shipments are subject to the import, licensing, prescription and regulatory requirements of the destination country. 5. How should Semaglutide be stored? Storage conditions vary by product. Buyers should follow the manufacturer's approved product information and cold-chain requirements. Why Choose MEDINDIA EXPORT? Pharmaceutical export support International trade inquiry assistance Product and documentation support Bulk pharmaceutical sourcing Worldwide shipping assistance, subject to destination-country regulations International Pharmaceutical Supply MEDINDIA EXPORT handles international pharmaceutical inquiries and supports customers with product sourcing and export requirements, subject to applicable regulations. 🌐 Website: www.medicineindiaexport.com 📧 Email: sales.medindiaexport@gmail.com 📱 WhatsApp: +91 7218129896

Product Name: Semaglutide Injection 2.4 mg Active Ingredient: Semaglutide Strength: 2.4 mg Dosage Form: Injection Route of Administration: Subcutaneous injection Therapeutic Category: Weight Management / GLP-1 Receptor Agonist Prescription Status: Prescription medicine Product Overview Semaglutide is a long-acting GLP-1 receptor agonist used in approved products for conditions including type 2 diabetes and chronic weight management, depending on the specific product and country. The 2.4 mg once-weekly maintenance dose is associated with Wegovy's approved weight-management regimen. Uses Depending on the approved product and local regulatory authorization, semaglutide may be used for: Chronic weight management in eligible adults Management of type 2 diabetes with specific semaglutide products Supporting reduction of appetite and food intake as part of an appropriate treatment program Important Safety Information Semaglutide should be used only under appropriate medical supervision. Important warnings and precautions include gastrointestinal adverse effects, pancreatitis, and contraindication in people with a personal or family history of medullary thyroid carcinoma (MTC) or MEN 2 for Wegovy. WHO has also warned about falsified semaglutide products and recommends obtaining these medicines through licensed/authorized supply channels and checking packaging, batch information and expiry dates. Storage & Handling Storage requirements depend on the specific manufacturer and presentation. Follow the manufacturer's approved product information and maintain the required cold-chain conditions for injectable semaglutide. Why Choose MEDINDIA EXPORT? Pharmaceutical export support International inquiry handling Product documentation support Worldwide shipping assistance, subject to destination-country regulations Support for bulk and business inquiries Quality-focused pharmaceutical sourcing Trading FAQs 1. What is Semaglutide Injection 2.4 mg? It is a semaglutide injection strength used as a maintenance dose in certain approved weight-management products. 2. Is semaglutide a prescription medicine? Yes. Semaglutide injections are prescription medicines, and requirements vary by country. 3. How is Semaglutide 2.4 mg administered? Approved 2.4 mg Wegovy maintenance dosing is administered subcutaneously once weekly. 4. Can semaglutide be exported internationally? International pharmaceutical shipments are subject to the import, prescription, registration and customs requirements of the destination country. 5. How should injectable semaglutide be sourced? Use authorized pharmaceutical supply channels and verify the manufacturer's details, batch number and expiry date. WHO specifically warns about falsified semaglutide products. 6. Is Semaglutide 2.4 mg available in every country? No. Product authorization, available strengths, brands and prescribing requirements differ between countries. International Pharmaceutical Supply MEDINDIA EXPORT supports pharmaceutical export inquiries for international markets, subject to applicable regulations, product authorization and import requirements in the destination country. 🌐 Website: www.medicineindiaexport.com 📧 Email: sales.medindiaexport@gmail.com 📱 WhatsApp: +91 7218129896

Product Information Product Details Generic Name Semaglutide Brand Name Poviztra® FlexTouch® Strength 0.25 mg Dosage Form Injection Pack Size 1.5 mL Presentation Pre-filled pen Administration Subcutaneous Frequency Once weekly* Pack Configuration 1 pen + 4 disposable needles Therapeutic Category GLP-1 Receptor Agonist / Diabetes & Metabolic Care Prescription Status Prescription medicine *The supplied packaging states once-weekly use. Dosing and indications must follow the approved product information for the relevant market. For example, current U.S. FDA labeling for semaglutide injection includes a 0.25 mg once-weekly starting dose for certain approved products. Product Description Semaglutide is a GLP-1 receptor agonist used in approved clinical settings. Depending on the specific semaglutide product and country's regulatory authorization, it may be indicated for type 2 diabetes, weight management, and other approved indications. The 0.25 mg strength is commonly used as an initiation dose in approved semaglutide injection regimens, followed by dose escalation according to the applicable prescribing information. Key Features Semaglutide 0.25 mg formulation Pre-filled injection pen Subcutaneous administration Once-weekly presentation shown on the supplied pack Convenient multi-dose pen presentation Suitable for pharmaceutical distribution subject to destination-country regulations Uses Semaglutide products may be prescribed for approved metabolic indications such as: Type 2 diabetes management Weight management in eligible patients, where authorized Other indications where specifically approved by the relevant regulatory authority The exact indication should always be confirmed against the local approved product information. Safety & Important Considerations Semaglutide is a prescription medicine and should be used under appropriate medical supervision. Important contraindications and warnings vary by product. Current FDA labeling for semaglutide injection includes contraindications involving a personal or family history of medullary thyroid carcinoma (MTC), MEN 2, or known hypersensitivity to semaglutide or its excipients. Potential adverse effects include gastrointestinal reactions such as nausea, vomiting, diarrhea and constipation; serious adverse reactions can also occur. International Pharmaceutical Export MEDINDIA EXPORT supports international pharmaceutical trading enquiries from buyers, distributors, pharmacies and healthcare businesses, subject to applicable export and import regulations. Target Countries & Markets USA: California, Texas, Florida, New York, Illinois, Pennsylvania, Ohio, Georgia, North Carolina, New Jersey, Virginia, Washington, Arizona, Massachusetts, Michigan UK: Greater London, Manchester, Birmingham, Liverpool, Sheffield, Bristol, Nottingham, Leicester, Southampton, Glasgow, Edinburgh, Cardiff, Belfast Singapore: Central Region, Marina Bay, CBD, Jurong East, Woodlands, Queenstown, Tampines, Bedok, Orchard, Novena Thailand: Bangkok, Chiang Mai, Phuket, Rayong, Chonburi, Nonthaburi, Samut Prakan, Pathum Thani, Khon Kaen, Udon Thani Malaysia: Kuala Lumpur, Selangor, Johor, Penang, Sarawak, Putrajaya, Johor Bahru, Petaling Jaya, George Town Australia: New South Wales, Victoria, Queensland, Western Australia, Sydney, Melbourne, Brisbane, Perth, Adelaide Other international markets: UAE, New Zealand and additional destinations, subject to local pharmaceutical regulations, import requirements and product authorization. Trading FAQs Q1. What is Semaglutide 0.25 mg? Semaglutide 0.25 mg is a low-strength semaglutide injection used as an initiation dose in certain approved treatment regimens. Q2. Is Semaglutide prescription-only? Yes. It should be supplied and used according to applicable prescription and pharmaceutical regulations. Q3. How is it administered? The supplied pack identifies it as a subcutaneous injection. Patients should follow their healthcare professional's instructions and the approved product information. Q4. Is 0.25 mg a maintenance dose? For several approved semaglutide injection regimens, 0.25 mg is an initiation dose rather than the maintenance dose. Dose escalation should be determined by the prescriber according to the specific product labeling. Q5. Can you supply internationally? International supply is subject to the destination country's import, registration, prescription and customs requirements. Q6. What should international buyers provide? Buyers should provide the required product, quantity, destination country and relevant business/import documentation so applicable requirements can be reviewed. Contact MEDINDIA EXPORT 🌐 Website: www.medicineindiaexport.com 📧 Email: sales.medindiaexport@gmail.com 📱 WhatsApp: +91 7218129896 MEDINDIA EXPORT – Pharmaceutical Export & International Trading

Product Name: Semaglutide Injection 0.5 mg Active Ingredient: Semaglutide Dosage Form: Injection Strength: 0.5 mg Category: Diabetes & Weight Management Medicines Therapeutic Class: GLP-1 receptor agonist Product Overview Semaglutide Injection 0.5 mg is a prescription medicine containing semaglutide. It is used under medical supervision for appropriate patients with type 2 diabetes and, depending on the specific approved product and indication, for weight-management treatment. Uses Helps improve blood-glucose control in eligible adults with type 2 diabetes. May be prescribed for chronic weight management for eligible patients when the specific product is approved for that indication. Used according to the prescribing information applicable in the destination country. Important Considerations Semaglutide is a prescription medicine and should be used only under the guidance of a qualified healthcare professional. Dosage, eligibility, contraindications, storage requirements, and approved indications can vary by product and country. International Supply MEDINDIA EXPORT provides pharmaceutical sourcing and international export services, subject to applicable prescription, import, customs, and regulatory requirements in the destination country. Target Markets: USA, UK, Singapore, Thailand, UAE, Australia, Malaysia, New Zealand, Canada, Germany, France, Italy, Spain, Netherlands, Sweden & Ireland. Trading FAQs Q1. Is Semaglutide Injection 0.5 mg a prescription medicine? Yes. Semaglutide products are prescription medicines and should be used under appropriate medical supervision. Q2. Can Semaglutide Injection 0.5 mg be exported internationally? International shipment depends on the destination country's pharmaceutical import regulations, prescription requirements, and customs rules. Q3. How should Semaglutide Injection be stored? Storage requirements depend on the specific product and manufacturer. Follow the product label and approved prescribing information. Q4. Can I order Semaglutide for another country? Availability and lawful import depend on the destination country's regulations. Customers should verify local requirements before placing an order. Q5. How can I request product availability and pricing? Contact our team with the required quantity and destination country for product availability, documentation, and quotation details. Contact MEDINDIA EXPORT 🌐 Website: www.medicineindiaexport.com 📧 Email: sales.medindiaexport@gmail.com 📱 WhatsApp: +91 7218129896

Product Name: U-Tryp 100,000 IU Injection Generic Name: Ulinastatin Strength: 100,000 IU Dosage Form: Injection Category: Critical Care / Specialty Pharmaceutical Route of Administration: As directed by a qualified healthcare professional Product Overview Ulinastatin for Injection 100,000 IU – U-Tryp is a specialty pharmaceutical injection containing ulinastatin. It is a protease inhibitor used in hospital and critical-care settings for specific clinical conditions according to the treating physician's assessment. U-Tryp is supplied as an injectable formulation intended for administration by qualified healthcare professionals. Product availability, indications, prescribing requirements, and import regulations may differ between countries. Uses Ulinastatin may be used under medical supervision for selected conditions where inhibition of certain proteolytic enzymes is clinically indicated. The appropriate indication, dosage, duration, and method of administration should be determined by a qualified healthcare professional. Key Product Features Ulinastatin injection formulation Strength: 100,000 IU Suitable for hospital and specialty-care requirements Intended for professional medical use Manufactured and supplied according to applicable pharmaceutical requirements Important Considerations Ulinastatin is a prescription medicine and should only be administered under appropriate medical supervision. Do not self-administer injectable medicines. Healthcare professionals should review the patient's medical history, concomitant medicines, contraindications, and applicable prescribing information before use. For international orders, importation and dispensing requirements can vary by destination country. Buyers and healthcare institutions should verify local regulatory requirements before placing an order. Storage Store the product according to the manufacturer's labeled storage conditions. Keep medicines in their original packaging and protect them from inappropriate temperature, moisture, and direct exposure as applicable. International Pharmaceutical Supply MEDINDIA EXPORT supplies pharmaceutical products for international B2B requirements and supports inquiries from customers across multiple international markets, subject to applicable export and import regulations. Target Markets: USA, UK, UAE, Singapore, Australia, Malaysia, Thailand, Canada, New Zealand, Germany, France, Italy, Spain, South Africa, Kenya, Nigeria, Philippines, and other international destinations. Trading FAQs Q1. What is U-Tryp 100,000 IU? U-Tryp 100,000 IU is an injectable formulation containing ulinastatin. Q2. What category does U-Tryp belong to? It belongs to the Critical Care / Specialty Pharmaceutical category. Q3. Who should administer U-Tryp? It should be administered by a qualified healthcare professional according to the prescribed treatment plan. Q4. Can U-Tryp be exported internationally? International supply is subject to the export regulations of the origin country and the import, registration, prescription, and customs requirements of the destination country. Q5. Can I request a quotation for U-Tryp? Yes. Contact MEDINDIA EXPORT with your required quantity and destination country to discuss availability and applicable shipping and documentation requirements. Q6. Is a prescription required? Requirements vary by country. Buyers should follow the prescription and regulatory requirements applicable in their jurisdiction. Request a Product Inquiry For availability, quotation, bulk pharmaceutical requirements, and international supply inquiries, contact: 🌐 Website: www.medicineindiaexport.com 📧 Email: sales.medindiaexport@gmail.com 📱 WhatsApp: +91 7218129896 MEDINDIA EXPORT – Pharmaceutical Export & International Supply

Product Name: Somatropin Injection 60 mg / 1.2 mL Active Ingredient: Somatropin (recombinant human growth hormone) Strength: 60 mg / 1.2 mL Dosage Form: Injection Therapeutic Category: Growth Hormone / Endocrinology Route: Subcutaneous injection Somatropin is a recombinant human growth hormone used in the management of specific growth hormone deficiencies and related growth disorders. Approved uses vary by product, strength, age group, and country. Uses Somatropin products may be prescribed for conditions involving growth hormone deficiency, including certain pediatric growth disorders and, for some products, adult growth hormone deficiency. Key Product Features Somatropin / recombinant human growth hormone 60 mg / 1.2 mL presentation Injectable dosage form Intended for use under healthcare-professional supervision Prescription medicine; regulatory status and approved indications differ by country Important Considerations Somatropin should be used only according to a qualified healthcare professional's prescription and the applicable product information. Dosing is individualized according to the indication, patient characteristics, and clinical response. Potential risks and precautions can include glucose intolerance, fluid retention, hypersensitivity, intracranial hypertension, and other product-specific adverse effects. Storage & Handling Storage requirements depend on the specific manufacturer and formulation. Follow the manufacturer's approved package insert and cold-chain requirements; do not assume storage conditions from another somatropin product. International Supply For international pharmaceutical enquiries, availability, documentation, shipping requirements, and import eligibility should be confirmed for the destination country before ordering. Somatropin is a prescription biologic and regulations differ between markets. Trading FAQs 1. What is Somatropin 60 mg / 1.2 mL? It is an injectable formulation containing recombinant human growth hormone (somatropin). 2. What category does Somatropin belong to? It belongs to the Growth Hormone / Endocrinology category. 3. Is Somatropin prescription-only? Somatropin is a prescription medicine in many markets. Local regulations should be checked before supply or import. 4. How is Somatropin administered? Somatropin products are administered by subcutaneous injection according to the specific product's prescribing information. 5. Can Somatropin be exported internationally? International supply depends on the destination country's pharmaceutical import regulations, prescription requirements, product registration, and applicable customs rules. 6. Can you provide product and shipping details? For current availability, packaging, documentation, and international quotation, contact our export team. Contact MEDINDIA EXPORT MEDINDIA EXPORT 🌐 Website: www.medicineindiaexport.com 📧 Email: sales.medindiaexport@gmail.com 📱 WhatsApp: +91 7218129896

Genryzon 24 mg/1.2 mL is a prescription growth-hormone therapy containing somatrogon, supplied as a prefilled injection pen for subcutaneous administration. Product Details Product Information Details Brand Name Genryzon Active Ingredient Somatrogon Strength 24 mg/1.2 mL Dosage Form Injection Presentation Prefilled pen Route Subcutaneous Therapeutic Category Growth Hormone / Endocrinology Prescription Status Prescription medicine Manufacturer/Brand Owner Pfizer Uses Somatrogon is used under medical supervision for appropriate pediatric patients with growth hormone deficiency and associated growth failure, according to the applicable approved product information. Product Highlights Somatrogon 24 mg/1.2 mL Convenient prefilled-pen presentation Long-acting growth hormone analogue Intended for subcutaneous administration Suitable for pharmaceutical trade inquiries, subject to destination-country regulations International Medicine Export MEDINDIA EXPORT provides pharmaceutical sourcing and export services for international customers. We handle inquiries for markets including: 🇺🇸 USA: California, Texas, Florida, New York, Illinois, Pennsylvania, Ohio, Georgia, North Carolina, New Jersey, Virginia, Washington, Arizona, Massachusetts, Michigan 🇬🇧 UK: London, Manchester, Birmingham, Liverpool, Sheffield, Bristol, Nottingham, Leicester, Southampton, Glasgow, Edinburgh, Cardiff, Belfast 🇸🇬 Singapore: Central Region, Marina Bay, CBD, Jurong East, Woodlands, Queenstown, Tampines, Bedok, Orchard, Novena 🇹🇭 Thailand: Bangkok, Chiang Mai, Phuket, Rayong, Chonburi, Nonthaburi, Samut Prakan, Pathum Thani, Khon Kaen, Udon Thani 🇲🇾 Malaysia: Kuala Lumpur, Selangor, Johor, Penang, Sarawak, Putrajaya, Johor Bahru, Petaling Jaya, George Town 🇦🇺 Australia: New South Wales, Victoria, Queensland, Western Australia, Sydney, Melbourne, Brisbane, Perth, Adelaide 🇳🇿 New Zealand and other international destinations, subject to applicable import regulations. Trading FAQs Q. What category does Genryzon belong to? Genryzon belongs to the Growth Hormone / Endocrinology category. Q. What is the active ingredient? The active ingredient is somatrogon. Q. What strength is available? This listing is for 24 mg/1.2 mL in a prefilled pen. Q. Is Genryzon prescription-only? Yes. It should be supplied and used according to applicable prescription and pharmaceutical regulations. Q. Can Genryzon be exported internationally? International supply depends on the regulations of the exporting and importing countries, including applicable prescription, import authorization and product-registration requirements. Q. How can I request a quotation? Contact MEDINDIA EXPORT with the required quantity and destination country for product availability and trade information. Request a Trade Inquiry 🌐 Website: www.medicineindiaexport.com 📧 Email: sales.medindiaexport@gmail.com 📱 WhatsApp: +91 7218129896