01 1CENTAUR PHARMACEUTICALS PRIVATE LIMITED Mumbai IN
02 1F.I.S. - Fabbrica Italiana Sintetici S.p.A. Montecchio Maggiore IT
03 1R.L. FINE CHEM PRIVATE LIMITED Chikkaballapur IN
01 3Oxazepam
01 1India
02 1Italy
03 1Blank
01 3Valid
Certificate Number : CEP 2008-283 - Rev 02
Status : Valid
Issue Date : 2023-10-19
Type : Chemical
Substance Number : 778
Certificate Number : CEP 2011-014 - Rev 02
Status : Valid
Issue Date : 2024-06-19
Type : Chemical
Substance Number : 778
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Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Certificate Number : CEP 2024-383 - Rev 00
Status : Valid
Issue Date : 2025-06-02
Type : Chemical
Substance Number : 778
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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PharmaCompass offers a list of Oxazepam 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 Oxazepam manufacturer or Oxazepam supplier for your needs.
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PharmaCompass also assists you with knowing the Oxazepam API Price utilized in the formulation of products. Oxazepam API Price is not always fixed or binding as the Oxazepam Price is obtained through a variety of data sources. The Oxazepam Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Anxiolit retard manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Anxiolit retard, including repackagers and relabelers. The FDA regulates Anxiolit retard manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Anxiolit retard API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Anxiolit retard supplier is an individual or a company that provides Anxiolit retard active pharmaceutical ingredient (API) or Anxiolit retard finished formulations upon request. The Anxiolit retard suppliers may include Anxiolit retard API manufacturers, exporters, distributors and traders.
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A Anxiolit retard CEP of the European Pharmacopoeia monograph is often referred to as a Anxiolit retard Certificate of Suitability (COS). The purpose of a Anxiolit retard CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Anxiolit retard EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Anxiolit retard to their clients by showing that a Anxiolit retard CEP has been issued for it. The manufacturer submits a Anxiolit retard CEP (COS) as part of the market authorization procedure, and it takes on the role of a Anxiolit retard CEP holder for the record. Additionally, the data presented in the Anxiolit retard CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Anxiolit retard DMF.
A Anxiolit retard CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Anxiolit retard CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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