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PharmaCompass offers a list of Nimodipine 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 Nimodipine manufacturer or Nimodipine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Nimodipine manufacturer or Nimodipine supplier.
PharmaCompass also assists you with knowing the Nimodipine API Price utilized in the formulation of products. Nimodipine API Price is not always fixed or binding as the Nimodipine Price is obtained through a variety of data sources. The Nimodipine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Alpharma Brand of Nimodipine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Alpharma Brand of Nimodipine, including repackagers and relabelers. The FDA regulates Alpharma Brand of Nimodipine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Alpharma Brand of Nimodipine 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 Alpharma Brand of Nimodipine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Alpharma Brand of Nimodipine supplier is an individual or a company that provides Alpharma Brand of Nimodipine active pharmaceutical ingredient (API) or Alpharma Brand of Nimodipine finished formulations upon request. The Alpharma Brand of Nimodipine suppliers may include Alpharma Brand of Nimodipine API manufacturers, exporters, distributors and traders.
click here to find a list of Alpharma Brand of Nimodipine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Alpharma Brand of Nimodipine DMF (Drug Master File) is a document detailing the whole manufacturing process of Alpharma Brand of Nimodipine active pharmaceutical ingredient (API) in detail. Different forms of Alpharma Brand of Nimodipine DMFs exist exist since differing nations have different regulations, such as Alpharma Brand of Nimodipine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Alpharma Brand of Nimodipine DMF submitted to regulatory agencies in the US is known as a USDMF. Alpharma Brand of Nimodipine USDMF includes data on Alpharma Brand of Nimodipine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Alpharma Brand of Nimodipine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Alpharma Brand of Nimodipine suppliers with USDMF 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 Alpharma Brand of Nimodipine Drug Master File in Korea (Alpharma Brand of Nimodipine KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Alpharma Brand of Nimodipine. The MFDS reviews the Alpharma Brand of Nimodipine KDMF as part of the drug registration process and uses the information provided in the Alpharma Brand of Nimodipine KDMF to evaluate the safety and efficacy of the drug.
After submitting a Alpharma Brand of Nimodipine 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 Alpharma Brand of Nimodipine API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Alpharma Brand of Nimodipine suppliers with KDMF on PharmaCompass.
A Alpharma Brand of Nimodipine CEP of the European Pharmacopoeia monograph is often referred to as a Alpharma Brand of Nimodipine Certificate of Suitability (COS). The purpose of a Alpharma Brand of Nimodipine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Alpharma Brand of Nimodipine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Alpharma Brand of Nimodipine to their clients by showing that a Alpharma Brand of Nimodipine CEP has been issued for it. The manufacturer submits a Alpharma Brand of Nimodipine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Alpharma Brand of Nimodipine CEP holder for the record. Additionally, the data presented in the Alpharma Brand of Nimodipine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Alpharma Brand of Nimodipine DMF.
A Alpharma Brand of Nimodipine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Alpharma Brand of Nimodipine CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Alpharma Brand of Nimodipine suppliers with CEP (COS) on PharmaCompass.
A Alpharma Brand of Nimodipine written confirmation (Alpharma Brand of Nimodipine WC) is an official document issued by a regulatory agency to a Alpharma Brand of Nimodipine manufacturer, verifying that the manufacturing facility of a Alpharma Brand of Nimodipine active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Alpharma Brand of Nimodipine APIs or Alpharma Brand of Nimodipine finished pharmaceutical products to another nation, regulatory agencies frequently require a Alpharma Brand of Nimodipine WC (written confirmation) as part of the regulatory process.
click here to find a list of Alpharma Brand of Nimodipine suppliers with Written Confirmation (WC) 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 Alpharma Brand of Nimodipine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Alpharma Brand of Nimodipine 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 Alpharma Brand of Nimodipine 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 Alpharma Brand of Nimodipine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Alpharma Brand of Nimodipine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Alpharma Brand of Nimodipine suppliers with NDC on PharmaCompass.
Alpharma Brand of Nimodipine 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 Alpharma Brand of Nimodipine 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 Alpharma Brand of Nimodipine GMP manufacturer or Alpharma Brand of Nimodipine GMP API supplier for your needs.
A Alpharma Brand of Nimodipine CoA (Certificate of Analysis) is a formal document that attests to Alpharma Brand of Nimodipine's compliance with Alpharma Brand of Nimodipine specifications and serves as a tool for batch-level quality control.
Alpharma Brand of Nimodipine CoA mostly includes findings from lab analyses of a specific batch. For each Alpharma Brand of Nimodipine 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.
Alpharma Brand of Nimodipine may be tested according to a variety of international standards, such as European Pharmacopoeia (Alpharma Brand of Nimodipine EP), Alpharma Brand of Nimodipine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Alpharma Brand of Nimodipine USP).