Insulin Degludec API Manufacturers & Suppliers
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Looking for Insulin Degludec API 844439-96-9?
- Description:
- Here you will find a list of producers, manufacturers and distributors of Insulin Degludec. You can filter on certificates such as GMP, FDA, CEP, Written Confirmation and more. Send inquiries for free and get in direct contact with the supplier of your choice.
- API | Excipient name:
- Insulin Degludec
- Cas Number:
- 844439-96-9
- DrugBank number:
- DB09564
- Unique Ingredient Identifier:
- NN-1250;NN1250
About Insulin Degludec
Insulin Degludec, marketed under brand names like Tresiba, is an ultra-long-acting form of insulin, used for the treatment of hyperglycemia caused by Type 1 and Type 2 Diabetes. Unlike conventional insulin, it has an added hexadecanedioic acid on lysine at the B29 position, facilitating the formation of multi-hexamers upon subcutaneous injection. This unique structure allows for a protracted action profile, providing a consistent level of basal insulin over 42 hours with a low peak: trough ratio. Insulin Degludec's effectiveness in glycemic control makes it a vital component in diabetes management, particularly benefiting patients requiring stable and prolonged insulin action.
Food & Drug Administration approved
The Food and Drug Administration is a federal agency of the United States Department of Health and Human Services, one of the United States federal executive departments. FDA is important because it is intended to have companies produce their goods to certain standards and it presents this fact in a clear overview using FDA certificates. When a company is (US) FDA approved, it shows the American government has declared the API or medicine as safe and it can be sold, imported, or used in the United States. The USA is not the only country with a regulatory agency like FDA. Most other countries have agencies that are responsible for the national safety of pharmaceutical products. Some different kinds of organizations include:
EMA (European Medicines Agency, European Union)
MHRA (Medicines and Healthcare products Regulatory Agency, United Kingdom)
PMDA (Pharmaceuticals and Medical Devices Agency, Japan)
CDSCO (Central Drugs Standard Control Organization, India)
