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Molecular Weight | 5917 g/mol |
---|---|
Molecular Formula | C267H402N64O76S6 |
XLogP3 | -3.5 |
Hydrogen Bond Donor Count | 76 |
Hydrogen Bond Acceptor Count | 87 |
Rotatable Bond Count | 189 |
Exact Mass | 5914.7950469 g/mol |
Monoisotopic Mass | 5912.7883372 g/mol |
Topological Polar Surface Area | 2400 Ų |
Heavy Atom Count | 413 |
Formal Charge | 0 |
Complexity | 14700 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 50 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 1 |
1 of 4 | |
---|---|
Drug Name | Levemir |
PubMed Health | Insulin Detemir (Injection) |
Drug Label | LEVEMIR (insulin detemir [rDNA origin] injection) is a sterile solution of insulin detemir for use as an injection. Insulin detemir is a long-acting basal insulin analog, with up to 24 hours duration of action, produced by a proceb that includes e... |
Active Ingredient | Insulin detemir recombinant; Insulin detemir |
Dosage Form | Injectable |
Route | injection; Subcutaneous |
Strength | 100 units/ml; 1000 units/10ml (100 units/ml) |
Market Status | Prescription |
Company | Novo Nordisk |
2 of 4 | |
---|---|
Drug Name | Levemir flexpen |
Active Ingredient | Insulin detemir recombinant |
Dosage Form | Injectable |
Route | Subcutaneous |
Strength | 300 units/3ml (100 units/ml) |
Market Status | Prescription |
Company | Novo Nordisk |
3 of 4 | |
---|---|
Drug Name | Levemir |
PubMed Health | Insulin Detemir (Injection) |
Drug Label | LEVEMIR (insulin detemir [rDNA origin] injection) is a sterile solution of insulin detemir for use as an injection. Insulin detemir is a long-acting basal insulin analog, with up to 24 hours duration of action, produced by a proceb that includes e... |
Active Ingredient | Insulin detemir recombinant; Insulin detemir |
Dosage Form | Injectable |
Route | injection; Subcutaneous |
Strength | 100 units/ml; 1000 units/10ml (100 units/ml) |
Market Status | Prescription |
Company | Novo Nordisk |
4 of 4 | |
---|---|
Drug Name | Levemir flexpen |
Active Ingredient | Insulin detemir recombinant |
Dosage Form | Injectable |
Route | Subcutaneous |
Strength | 300 units/3ml (100 units/ml) |
Market Status | Prescription |
Company | Novo Nordisk |
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ABOUT THIS PAGE
A Insulin Detemir manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Insulin Detemir, including repackagers and relabelers. The FDA regulates Insulin Detemir manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Insulin Detemir API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Insulin Detemir manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Insulin Detemir supplier is an individual or a company that provides Insulin Detemir active pharmaceutical ingredient (API) or Insulin Detemir finished formulations upon request. The Insulin Detemir suppliers may include Insulin Detemir API manufacturers, exporters, distributors and traders.
click here to find a list of Insulin Detemir suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
Insulin Detemir Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.
GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).
PharmaCompass offers a list of Insulin Detemir GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Insulin Detemir GMP manufacturer or Insulin Detemir GMP API supplier for your needs.
A Insulin Detemir CoA (Certificate of Analysis) is a formal document that attests to Insulin Detemir's compliance with Insulin Detemir specifications and serves as a tool for batch-level quality control.
Insulin Detemir CoA mostly includes findings from lab analyses of a specific batch. For each Insulin Detemir CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.
Insulin Detemir may be tested according to a variety of international standards, such as European Pharmacopoeia (Insulin Detemir EP), Insulin Detemir JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Insulin Detemir USP).
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