High-Quality Semaglutide long-acting GLP-1 receptor agonist peptide API with white to off-white lyophilized powder Products, Product

Product Overview

Semaglutide is a long-acting GLP-1 receptor agonist peptide API, widely used for type 2 diabetes glycemic control and chronic weight management. It offers once-weekly dosing, strong efficacy, and well-established safety, making it one of the most in-demand generic APIs .

Product Description

Basic Information

CAS Number:910463-68-2
Molecular Formula:C187H291N45O59
Appearance:White to off-white lyophilized powder
Key Feature:Long half-life, once-weekly subcutaneous administration

Main Indications (Formulation Use)

  • Adjunct to diet and exercise for glycemic control in adults with type 2 diabetes mellitus
  • Chronic weight management in adults with obesity or overweight with weight-related comorbidities
  • Cardiovascular risk reduction in eligible diabetic patients

Quality Highlights

  • Purity: ≥99.0% by HPLC, strict impurity control
  • Manufactured under cGMP guidelines
  • Full batch records and stability data available
  • Suitable for injectable generic development

Storage Condition

Store in tightly sealed containers, protected from light and moisture, at -20°C frozen conditions. Avoid repeated freeze-thaw cycles.

Frequently Asked Questions

Q: What is the purity level of this product? A: The product maintains a high purity level of ≥99.0% as verified by HPLC analysis, ensuring strict control over impurities.
Q: What are the primary storage requirements? A: It should be stored in a frozen environment at -20°C. It is crucial to keep the containers tightly sealed and protected from both light and moisture.
Q: For which clinical indications is this formulation typically used? A: It is primarily used for glycemic control in type 2 diabetes, chronic weight management for obesity/overweight, and reducing cardiovascular risks in diabetic patients.
Q: Is this product suitable for pharmaceutical development? A: Yes, it is manufactured under cGMP guidelines and is specifically suitable for injectable generic development, with full stability data available.
Q: What is the administration frequency of the final formulation? A: Due to its long half-life, the resulting formulation is designed for once-weekly subcutaneous administration.
Q: Should I be concerned about freeze-thaw cycles? A: Yes, to maintain the integrity and stability of the lyophilized powder, you should avoid repeated freeze-thaw cycles.

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