EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
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01 1EUROAPI FRANCE Vertolaye FR
02 1EUROAPI GERMANY GmbH Frankfurt am Main DE
03 1CENTAUR PHARMACEUTICALS PRIVATE LIMITED Mumbai IN
04 1HONOUR LAB LIMITED Hyderabad IN
05 1MICRO LABS LIMITED Bengaluru IN
06 1MSN LIFE SCIENCES PRIVATE LIMITED Chandampet Village IN
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01 5Clobazam
02 1Clobazam, Micronised
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01 2France
02 4India
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01 6Valid
Certificate Number : R1-CEP 2004-314 - Rev 01
Status : Valid
Issue Date : 2022-02-08
Type : Chemical
Substance Number : 1974
Certificate Number : R1-CEP 2016-281 - Rev 00
Status : Valid
Issue Date : 2022-02-16
Type : Chemical
Substance Number : 1974
Certificate Number : CEP 2004-118 - Rev 04
Status : Valid
Issue Date : 2023-10-19
Type : Chemical
Substance Number : 1974
Certificate Number : R1-CEP 2016-237 - Rev 00
Status : Valid
Issue Date : 2023-02-13
Type : Chemical
Substance Number : 1974
Certificate Number : CEP 2019-168 - Rev 02
Status : Valid
Issue Date : 2024-10-14
Type : Chemical
Substance Number : 1974
Certificate Number : R1-CEP 2016-322 - Rev 00
Status : Valid
Issue Date : 2023-07-18
Type : Chemical
Substance Number : 1974
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PharmaCompass offers a list of Clobazam 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 Clobazam manufacturer or Clobazam supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Clobazam manufacturer or Clobazam supplier.
PharmaCompass also assists you with knowing the Clobazam API Price utilized in the formulation of products. Clobazam API Price is not always fixed or binding as the Clobazam Price is obtained through a variety of data sources. The Clobazam Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Mystan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mystan, including repackagers and relabelers. The FDA regulates Mystan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mystan 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 Mystan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Mystan supplier is an individual or a company that provides Mystan active pharmaceutical ingredient (API) or Mystan finished formulations upon request. The Mystan suppliers may include Mystan API manufacturers, exporters, distributors and traders.
click here to find a list of Mystan suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Mystan CEP of the European Pharmacopoeia monograph is often referred to as a Mystan Certificate of Suitability (COS). The purpose of a Mystan CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Mystan EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Mystan to their clients by showing that a Mystan CEP has been issued for it. The manufacturer submits a Mystan CEP (COS) as part of the market authorization procedure, and it takes on the role of a Mystan CEP holder for the record. Additionally, the data presented in the Mystan CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Mystan DMF.
A Mystan CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Mystan 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 Mystan suppliers with CEP (COS) on PharmaCompass.
We have 5 companies offering Mystan
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