Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
01 1BIOPHORE INDIA PHARMACEUTICALS PVT. LTD. Hyderabad IN
02 1LUSOCHIMICA S.P.A. Lomagna IT
03 1SIEGFRIED LTD Zofingen CH
04 1Union Quimico Farmaceutica, S.A. (Uquifa S.A.) Barcelona ES
01 4Nimodipine
01 1India
02 1Italy
03 1Spain
04 1Switzerland
01 3Valid
02 1Withdrawn by Holder
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
Certificate Number : R0-CEP 2020-353 - Rev 00
Status : Valid
Issue Date : 2022-10-25
Type : Chemical
Substance Number : 1245
Certificate Number : CEP 2022-403 - Rev 00
Status : Valid
Issue Date : 2024-01-24
Type : Chemical
Substance Number : 1245
Certificate Number : R0-CEP 1999-105 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2004-12-06
Type : Chemical
Substance Number : 1245
Certificate Number : CEP 2004-272 - Rev 03
Status : Valid
Issue Date : 2023-10-04
Type : Chemical
Substance Number : 1245
32
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 N0896 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of N0896, including repackagers and relabelers. The FDA regulates N0896 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. N0896 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 N0896 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A N0896 supplier is an individual or a company that provides N0896 active pharmaceutical ingredient (API) or N0896 finished formulations upon request. The N0896 suppliers may include N0896 API manufacturers, exporters, distributors and traders.
click here to find a list of N0896 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A N0896 CEP of the European Pharmacopoeia monograph is often referred to as a N0896 Certificate of Suitability (COS). The purpose of a N0896 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of N0896 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of N0896 to their clients by showing that a N0896 CEP has been issued for it. The manufacturer submits a N0896 CEP (COS) as part of the market authorization procedure, and it takes on the role of a N0896 CEP holder for the record. Additionally, the data presented in the N0896 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the N0896 DMF.
A N0896 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. N0896 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 N0896 suppliers with CEP (COS) on PharmaCompass.
We have 4 companies offering N0896
Get in contact with the supplier of your choice:
