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Molecular Weight | 5823 g/mol |
---|---|
Molecular Formula | C258H384N64O78S6 |
XLogP3 | -12.1 |
Hydrogen Bond Donor Count | 78 |
Hydrogen Bond Acceptor Count | 90 |
Rotatable Bond Count | 180 |
Exact Mass | 5820.6440255 g/mol |
Monoisotopic Mass | 5818.6373159 g/mol |
Topological Polar Surface Area | 2450 Ų |
Heavy Atom Count | 406 |
Formal Charge | 0 |
Complexity | 14600 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 52 |
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 | Apidra |
Drug Label | APIDRA (insulin glulisine [rDNA origin] injection) is a rapid-acting human insulin analog used to lower blood glucose. Insulin glulisine is produced by recombinant DNA technology utilizing a non-pathogenic laboratory strain of Escherichia coli (K12... |
Active Ingredient | Insulin glulisine recombinant |
Dosage Form | Injectable |
Route | Iv (infusion), subcutaneous |
Strength | 300 units/3ml (100 units/ml); 1000 units/10ml (100 units/ml) |
Market Status | Prescription |
Company | Sanofi Aventis Us |
2 of 4 | |
---|---|
Drug Name | Apidra solostar |
PubMed Health | Insulin Glulisine (Injection) |
Drug Classes | Antidiabetic |
Drug Label | APIDRA (insulin glulisine [rDNA origin] injection) is a rapid-acting human insulin analog used to lower blood glucose. Insulin glulisine is produced by recombinant DNA technology utilizing a non-pathogenic laboratory strain of Escherichia coli (K12... |
Active Ingredient | Insulin glulisine recombinant |
Dosage Form | Injectable |
Route | Subcutaneous |
Strength | 300 units/3ml |
Market Status | Prescription |
Company | Sanofi Aventis Us |
3 of 4 | |
---|---|
Drug Name | Apidra |
Drug Label | APIDRA (insulin glulisine [rDNA origin] injection) is a rapid-acting human insulin analog used to lower blood glucose. Insulin glulisine is produced by recombinant DNA technology utilizing a non-pathogenic laboratory strain of Escherichia coli (K12... |
Active Ingredient | Insulin glulisine recombinant |
Dosage Form | Injectable |
Route | Iv (infusion), subcutaneous |
Strength | 300 units/3ml (100 units/ml); 1000 units/10ml (100 units/ml) |
Market Status | Prescription |
Company | Sanofi Aventis Us |
4 of 4 | |
---|---|
Drug Name | Apidra solostar |
PubMed Health | Insulin Glulisine (Injection) |
Drug Classes | Antidiabetic |
Drug Label | APIDRA (insulin glulisine [rDNA origin] injection) is a rapid-acting human insulin analog used to lower blood glucose. Insulin glulisine is produced by recombinant DNA technology utilizing a non-pathogenic laboratory strain of Escherichia coli (K12... |
Active Ingredient | Insulin glulisine recombinant |
Dosage Form | Injectable |
Route | Subcutaneous |
Strength | 300 units/3ml |
Market Status | Prescription |
Company | Sanofi Aventis Us |
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PharmaCompass offers a list of Insulin Glulisine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Insulin Glulisine manufacturer or Insulin Glulisine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Insulin Glulisine manufacturer or Insulin Glulisine supplier.
PharmaCompass also assists you with knowing the Insulin Glulisine API Price utilized in the formulation of products. Insulin Glulisine API Price is not always fixed or binding as the Insulin Glulisine Price is obtained through a variety of data sources. The Insulin Glulisine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 207748-29-6 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 207748-29-6, including repackagers and relabelers. The FDA regulates 207748-29-6 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 207748-29-6 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A 207748-29-6 supplier is an individual or a company that provides 207748-29-6 active pharmaceutical ingredient (API) or 207748-29-6 finished formulations upon request. The 207748-29-6 suppliers may include 207748-29-6 API manufacturers, exporters, distributors and traders.
207748-29-6 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 207748-29-6 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 207748-29-6 GMP manufacturer or 207748-29-6 GMP API supplier for your needs.
A 207748-29-6 CoA (Certificate of Analysis) is a formal document that attests to 207748-29-6's compliance with 207748-29-6 specifications and serves as a tool for batch-level quality control.
207748-29-6 CoA mostly includes findings from lab analyses of a specific batch. For each 207748-29-6 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.
207748-29-6 may be tested according to a variety of international standards, such as European Pharmacopoeia (207748-29-6 EP), 207748-29-6 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (207748-29-6 USP).