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1. Dtxsid10151274
Molecular Weight | 5832 g/mol |
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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 | |
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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 |
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Importing Country | Total Quantity (KGS) |
Average Price (USD/KGS) |
Number of Transactions |
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Regulatory Info :
Registration Country : Italy
Brand Name : Novorapidfill
Dosage Form : Insulin Aspart 300Iu 3Ml 5 Units Parenteral Use
Dosage Strength : 5 cartridges SC 300 IU 3 ml
Packaging :
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Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Brand Name : Novorapid Flexpen
Dosage Form : Insulin Aspart 300Iu 3Ml 5 Units Parenteral Use
Dosage Strength : 5 cartridges SC in pens preriemp 3 ml 100 U/ml
Packaging :
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Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Brand Name : Novomix
Dosage Form : Soluble Insulin Aspart+Insulin Aspart Crystallised Protamino 50/50 300Iu 3Ml 5 Units Parenteral Use
Dosage Strength : FLEXPEN 5 cartridges SC in pens preriemp 3 ml 100 IU/ml
Packaging :
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Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Norway
Brand Name : Novomix Flexpen 30 100 E/ml
Dosage Form : Injection fluid, suspension
Dosage Strength : 100 IE/ml
Packaging : Finish filled pen
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Brand Name : Novo rapid Flexpen
Dosage Form : Injection fluid, resolution in the finished filled pen
Dosage Strength : 100 E/ml
Packaging : Finish filled pen
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Brand Name : Novo rapid Penfill
Dosage Form : Injection fluid, resolution in sylinderampulle
Dosage Strength : 100 E/ml
Packaging : Sylinderampulle
Approval Date :
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Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Switzerland
Brand Name : Fiasp
Dosage Form : Inj Loose
Dosage Strength : 100U/ml
Packaging :
Approval Date :
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Regulatory Info :
Registration Country : Switzerland
Regulatory Info :
Registration Country : Switzerland
Brand Name : Fiasp PumpCart
Dosage Form : Inj Loose
Dosage Strength : 100U/ml
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Switzerland
Regulatory Info :
Registration Country : Switzerland
Brand Name : Insulin NovoRapid Flextouch
Dosage Form : Inj Loose
Dosage Strength :
Packaging :
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Regulatory Info :
Registration Country : Switzerland
Regulatory Info :
Registration Country : Switzerland
Brand Name : Insulin NovoRapid PumpCart
Dosage Form : Inj Sol
Dosage Strength : 100U/ml
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Switzerland
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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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Insulin aspart manufacturer or Insulin aspart supplier.
PharmaCompass also assists you with knowing the Insulin aspart API Price utilized in the formulation of products. Insulin aspart API Price is not always fixed or binding as the Insulin aspart Price is obtained through a variety of data sources. The Insulin aspart Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A NovoMix manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of NovoMix, including repackagers and relabelers. The FDA regulates NovoMix manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. NovoMix 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 supplier is an individual or a company that provides NovoMix active pharmaceutical ingredient (API) or NovoMix finished formulations upon request. The NovoMix suppliers may include NovoMix API manufacturers, exporters, distributors and traders.
click here to find a list of NovoMix suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A NovoMix DMF (Drug Master File) is a document detailing the whole manufacturing process of NovoMix active pharmaceutical ingredient (API) in detail. Different forms of NovoMix DMFs exist exist since differing nations have different regulations, such as NovoMix USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A NovoMix DMF submitted to regulatory agencies in the US is known as a USDMF. NovoMix USDMF includes data on NovoMix's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The NovoMix USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of NovoMix 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 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for NovoMix 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 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 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a NovoMix NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of NovoMix suppliers with NDC on PharmaCompass.
NovoMix 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 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 GMP manufacturer or NovoMix GMP API supplier for your needs.
A NovoMix CoA (Certificate of Analysis) is a formal document that attests to NovoMix's compliance with NovoMix specifications and serves as a tool for batch-level quality control.
NovoMix CoA mostly includes findings from lab analyses of a specific batch. For each NovoMix 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 may be tested according to a variety of international standards, such as European Pharmacopoeia (NovoMix EP), NovoMix JP (Japanese Pharmacopeia) and the US Pharmacopoeia (NovoMix USP).