Nagpur, Maharashtra, India
+919730867604
 Nagpur, Maharashtra, India
+919730867604
+917218129896
Antiparasitic medicine

Semaglutide Injection 0.25 mg In USA, UK, Australia, Singapore, Thailand, Malaysia

In stockcod not available
Phone Number

+919730867604

Mon-Thu: 10 AM - 2 PM • Fri: 3 PM - 7AM

Address KDK College Road , Darshan Colony , Nandanvan, Nagpur, Maharashtra, India

Nagpur, Maharashtra, India, India, 440024

Description

Product Information Product Details Generic Name Semaglutide Brand Name Poviztraยฎ FlexTouchยฎ 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 ๐ŸŒ Website: www.medicineindiaexport.com ๐Ÿ“ง Email: sales.medindiaexport@gmail.com ๐Ÿ“ฑ WhatsApp: +91 7218129896 MEDINDIA EXPORT โ€“ Pharmaceutical Export & International Trading

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