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1. Dtxsid10151274
Molecular Weight | 5832 g/mol |
---|---|
Molecular Formula | C256H387N65O79S6 |
Hydrogen Bond Donor Count | 86 |
Hydrogen Bond Acceptor Count | 91 |
Rotatable Bond Count | 188 |
Exact Mass | 5829.6654893 g/mol |
Monoisotopic Mass | 5827.6587796 g/mol |
Topological Polar Surface Area | 2350 Ų |
Heavy Atom Count | 406 |
Formal Charge | 0 |
Complexity | 13000 |
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 | 2 |
1 of 2 | |
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Drug Name | Novolog |
PubMed Health | Insulin Aspart Protamine/Insulin Aspart (Injection) |
Drug Classes | Antidiabetic |
Drug Label | NovoLog Mix 70/30 (70% insulin aspart protamine suspension and 30% insulin aspart injection, [rDNA origin]) is a human insulin analog suspension containing 70% insulin aspart protamine crystals and 30% soluble insulin aspart. NovoLog Mix 70/30 is a b... |
Active Ingredient | Insulin aspart recombinant |
Dosage Form | Injectable |
Route | Subcutaneous |
Strength | 1000 units/10ml (100 units/ml) |
Market Status | Prescription |
Company | Novo Nordisk |
2 of 2 | |
---|---|
Drug Name | Novolog |
PubMed Health | Insulin Aspart Protamine/Insulin Aspart (Injection) |
Drug Classes | Antidiabetic |
Drug Label | NovoLog Mix 70/30 (70% insulin aspart protamine suspension and 30% insulin aspart injection, [rDNA origin]) is a human insulin analog suspension containing 70% insulin aspart protamine crystals and 30% soluble insulin aspart. NovoLog Mix 70/30 is a b... |
Active Ingredient | Insulin aspart recombinant |
Dosage Form | Injectable |
Route | Subcutaneous |
Strength | 1000 units/10ml (100 units/ml) |
Market Status | Prescription |
Company | Novo Nordisk |
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PharmaCompass offers a list of Insulin aspart 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 aspart manufacturer or Insulin aspart supplier for your needs.
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A NovoMix 30 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of NovoMix 30, including repackagers and relabelers. The FDA regulates NovoMix 30 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. NovoMix 30 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 NovoMix 30 supplier is an individual or a company that provides NovoMix 30 active pharmaceutical ingredient (API) or NovoMix 30 finished formulations upon request. The NovoMix 30 suppliers may include NovoMix 30 API manufacturers, exporters, distributors and traders.
click here to find a list of NovoMix 30 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A NovoMix 30 DMF (Drug Master File) is a document detailing the whole manufacturing process of NovoMix 30 active pharmaceutical ingredient (API) in detail. Different forms of NovoMix 30 DMFs exist exist since differing nations have different regulations, such as NovoMix 30 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A NovoMix 30 DMF submitted to regulatory agencies in the US is known as a USDMF. NovoMix 30 USDMF includes data on NovoMix 30's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The NovoMix 30 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of NovoMix 30 suppliers with USDMF on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing NovoMix 30 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for NovoMix 30 API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture NovoMix 30 as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain NovoMix 30 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a NovoMix 30 NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of NovoMix 30 suppliers with NDC on PharmaCompass.
NovoMix 30 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 NovoMix 30 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 NovoMix 30 GMP manufacturer or NovoMix 30 GMP API supplier for your needs.
A NovoMix 30 CoA (Certificate of Analysis) is a formal document that attests to NovoMix 30's compliance with NovoMix 30 specifications and serves as a tool for batch-level quality control.
NovoMix 30 CoA mostly includes findings from lab analyses of a specific batch. For each NovoMix 30 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.
NovoMix 30 may be tested according to a variety of international standards, such as European Pharmacopoeia (NovoMix 30 EP), NovoMix 30 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (NovoMix 30 USP).