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1. Q409935
Molecular Weight | 536.5 g/mol |
---|---|
Molecular Formula | C20H40N3NaO10P |
Hydrogen Bond Donor Count | 4 |
Hydrogen Bond Acceptor Count | 10 |
Rotatable Bond Count | 22 |
Exact Mass | 536.23490076 g/mol |
Monoisotopic Mass | 536.23490076 g/mol |
Topological Polar Surface Area | 171 Ų |
Heavy Atom Count | 35 |
Formal Charge | 0 |
Complexity | 623 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 1 |
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 | Macugen |
PubMed Health | Pegaptanib (Injection) |
Drug Classes | Ophthalmologic Agent |
Active Ingredient | Pegaptanib sodium |
Dosage Form | Injectable |
Route | Intravitreal |
Strength | eq 0.3mg acid/0.09ml |
Market Status | Prescription |
Company | Valeant Pharms |
2 of 2 | |
---|---|
Drug Name | Macugen |
PubMed Health | Pegaptanib (Injection) |
Drug Classes | Ophthalmologic Agent |
Active Ingredient | Pegaptanib sodium |
Dosage Form | Injectable |
Route | Intravitreal |
Strength | eq 0.3mg acid/0.09ml |
Market Status | Prescription |
Company | Valeant Pharms |
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PharmaCompass offers a list of Macugen 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 Macugen manufacturer or Macugen supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Macugen manufacturer or Macugen supplier.
PharmaCompass also assists you with knowing the Macugen API Price utilized in the formulation of products. Macugen API Price is not always fixed or binding as the Macugen Price is obtained through a variety of data sources. The Macugen Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Pegaptanib Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pegaptanib Sodium, including repackagers and relabelers. The FDA regulates Pegaptanib Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pegaptanib Sodium 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 Pegaptanib Sodium supplier is an individual or a company that provides Pegaptanib Sodium active pharmaceutical ingredient (API) or Pegaptanib Sodium finished formulations upon request. The Pegaptanib Sodium suppliers may include Pegaptanib Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Pegaptanib Sodium suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Pegaptanib Sodium Drug Master File in Korea (Pegaptanib Sodium KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Pegaptanib Sodium. The MFDS reviews the Pegaptanib Sodium KDMF as part of the drug registration process and uses the information provided in the Pegaptanib Sodium KDMF to evaluate the safety and efficacy of the drug.
After submitting a Pegaptanib Sodium KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Pegaptanib Sodium API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Pegaptanib Sodium suppliers with KDMF on PharmaCompass.
Pegaptanib Sodium 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 Pegaptanib Sodium 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 Pegaptanib Sodium GMP manufacturer or Pegaptanib Sodium GMP API supplier for your needs.
A Pegaptanib Sodium CoA (Certificate of Analysis) is a formal document that attests to Pegaptanib Sodium's compliance with Pegaptanib Sodium specifications and serves as a tool for batch-level quality control.
Pegaptanib Sodium CoA mostly includes findings from lab analyses of a specific batch. For each Pegaptanib Sodium 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.
Pegaptanib Sodium may be tested according to a variety of international standards, such as European Pharmacopoeia (Pegaptanib Sodium EP), Pegaptanib Sodium JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Pegaptanib Sodium USP).