01 1CENTAUR PHARMACEUTICALS PRIVATE LIMITED Mumbai IN
02 1MYLAN LABORATORIES LIMITED Hyderabad IN
01 2Temazepam
01 1India
02 1U.S.A
01 2Withdrawn by Holder
Certificate Number : CEP 2010-282 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2023-10-19
Type : Chemical
Substance Number : 954
Certificate Number : R0-CEP 2010-003 - Rev 03
Status : Withdrawn by Holder
Issue Date : 2014-09-30
Type : Chemical
Substance Number : 954
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PharmaCompass offers a list of Temazepam 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 Temazepam manufacturer or Temazepam supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Temazepam manufacturer or Temazepam supplier.
PharmaCompass also assists you with knowing the Temazepam API Price utilized in the formulation of products. Temazepam API Price is not always fixed or binding as the Temazepam Price is obtained through a variety of data sources. The Temazepam Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Uvamin Retard manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Uvamin Retard, including repackagers and relabelers. The FDA regulates Uvamin Retard manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Uvamin 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 Uvamin Retard supplier is an individual or a company that provides Uvamin Retard active pharmaceutical ingredient (API) or Uvamin Retard finished formulations upon request. The Uvamin Retard suppliers may include Uvamin Retard API manufacturers, exporters, distributors and traders.
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A Uvamin Retard CEP of the European Pharmacopoeia monograph is often referred to as a Uvamin Retard Certificate of Suitability (COS). The purpose of a Uvamin Retard CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Uvamin Retard EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Uvamin Retard to their clients by showing that a Uvamin Retard CEP has been issued for it. The manufacturer submits a Uvamin Retard CEP (COS) as part of the market authorization procedure, and it takes on the role of a Uvamin Retard CEP holder for the record. Additionally, the data presented in the Uvamin Retard CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Uvamin Retard DMF.
A Uvamin Retard CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Uvamin Retard 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 Uvamin Retard suppliers with CEP (COS) on PharmaCompass.
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