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PharmaCompass offers a list of Amlodipine Besylate 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 Amlodipine Besylate manufacturer or Amlodipine Besylate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Amlodipine Besylate manufacturer or Amlodipine Besylate supplier.
PharmaCompass also assists you with knowing the Amlodipine Besylate API Price utilized in the formulation of products. Amlodipine Besylate API Price is not always fixed or binding as the Amlodipine Besylate Price is obtained through a variety of data sources. The Amlodipine Besylate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A EXFORGE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of EXFORGE, including repackagers and relabelers. The FDA regulates EXFORGE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. EXFORGE 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 EXFORGE manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A EXFORGE supplier is an individual or a company that provides EXFORGE active pharmaceutical ingredient (API) or EXFORGE finished formulations upon request. The EXFORGE suppliers may include EXFORGE API manufacturers, exporters, distributors and traders.
click here to find a list of EXFORGE suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A EXFORGE CEP of the European Pharmacopoeia monograph is often referred to as a EXFORGE Certificate of Suitability (COS). The purpose of a EXFORGE CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of EXFORGE EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of EXFORGE to their clients by showing that a EXFORGE CEP has been issued for it. The manufacturer submits a EXFORGE CEP (COS) as part of the market authorization procedure, and it takes on the role of a EXFORGE CEP holder for the record. Additionally, the data presented in the EXFORGE CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the EXFORGE DMF.
A EXFORGE CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. EXFORGE 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 EXFORGE suppliers with CEP (COS) on PharmaCompass.
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