About Glimepiride Api Powder
Product Specification
| CAS Number |
93479-97-1 |
| Formula: C24H34N4O5S |
C24H34N4O5S |
| Purity |
99 % |
| Treatment |
Treat high blood sugar levels caused by type 2 diabetes |
| GRADE |
IP/BP/USP |
| Minimum Order Quantity |
20 Kg |
Product Description
Product Description
Glimepirideiis an orally available medium-to-long acting sulfonylurea antidiabetic drug. Glimepiride is indicated to treat type 2 diabetes mellitus; its mode of action is to increase insulin production by the pancreas. Its use is contraindicated in patients with hypersensitivity to glimepiride or other sulfonylureas.
It lowers blood sugar by stimulating the release of insulin by pancreatic beta cells and by inducing increased activity of intracellular insulin receptors.Exports To:iGeorgia | Palestinian National Authority | Latvia | Japan | Iraq
Additional Information
| Delivery Time |
week |
| Production Capacity |
2500 |
| Packaging Details |
1kg to 25 kg |
Exceptional Purity and Quality AssuranceGlimepiride API Powder offers a purity greater than 99%, meeting rigorous USP/BP standards for pharmaceuticals. With strictly limited impurities and tight microbial controls, it ensures a safe and reliable product suitable for critical pharmaceutical formulation. Regular quality reviews and adherence to GMP guidelines underpin its consistent performance.
Efficiently Packed and Safe for Global ShipmentOur Glimepiride API Powder is carefully packed in double-layer LDPE bags fitted inside robust HDPE drums. This protective packaging maintains the product's stability by shielding it from moisture, light, and contamination, ensuring it arrives safely and intact for use by global suppliers, manufacturers, and importers.
Optimized for Specialized Pharmaceutical UseDesigned specifically for pharmaceutical manufacturing, Glimepiride API Powder is mainly used as an active antidiabetic ingredient. Its precise particle size and dependable chemical properties streamline production processes and enhance medication quality for patients managing type 2 diabetes.
FAQ's of Glimepiride Api Powder:
Q: How is the purity and quality of Glimepiride API Powder ensured?
A: Glimepiride API Powder is manufactured under stringent GMP (Good Manufacturing Practice) compliance, with purity exceeding 99%. The product conforms to USP/BP standards, with single and total impurities kept below 0.1% and 0.3%, respectively, and undergoes thorough quality testing for microbial limits and other key parameters.
Q: What is the recommended process for storing Glimepiride API Powder?
A: To maintain its stability, Glimepiride API Powder should be stored in a tightly closed container, away from light, moisture, and excessive heat. The original double LDPE bags inside HDPE drums provide optimal protection during storage.
Q: When should Glimepiride API Powder be used in pharmaceutical production?
A: Glimepiride API Powder is suitable for use in the formulation of antidiabetic medications at any production phase where the incorporation of an active pharmaceutical ingredient (API) is required. It is typically integrated during the active ingredient blending process of oral antidiabetic drug manufacturing.
Q: Where is the Glimepiride API Powder manufactured and supplied from?
A: Our Glimepiride API Powder is produced in India by GMP-certified facilities and is available for export, import, and local supply. The secure packaging facilitates safe transport to both domestic and international pharmaceutical manufacturers.
Q: What are the key benefits of using Glimepiride API Powder in drug formulations?
A: The high purity, low impurity profile, and strict microbial limits of Glimepiride API Powder ensure the safety and effectiveness of the final medication. Its consistent quality and compliance with pharmacopoeial standards make it an ideal choice for producing safe treatments for type 2 diabetes mellitus.
Q: How is the physical integrity of the powder ensured during shipping?
A: Glimepiride API Powder is packed in double LDPE bags, sealed within HDPE drums, which protect it from contamination, environmental factors, and damage during transit, ensuring the product maintains its quality upon delivery.