01 1Chemische Fabrik Berg GmbH Bitterfeld-Wolfen DE
02 1SCI PHARMTECH, INC. Taoyuan City TW
01 2Pentobarbital Sodium
01 1Germany
02 1Taiwan
01 2Valid
Certificate Number : R1-CEP 2002-061 - Rev 03
Status : Valid
Issue Date : 2019-03-21
Type : Chemical
Substance Number : 419
SCI Pharmtech offers high-quality, cost-effective APIs, advanced intermediates, & custom products with global expertise and precision.
SCI Pharmtech offers high-quality, cost-effective APIs, advanced intermediates, & custom products with global expertise and precision.
Certificate Number : R1-CEP 2009-030 - Rev 04
Status : Valid
Issue Date : 2020-11-25
Type : Chemical
Substance Number : 419
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PharmaCompass offers a list of Pentobarbital Sodium 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 Pentobarbital Sodium manufacturer or Pentobarbital Sodium supplier for your needs.
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PharmaCompass also assists you with knowing the Pentobarbital Sodium API Price utilized in the formulation of products. Pentobarbital Sodium API Price is not always fixed or binding as the Pentobarbital Sodium Price is obtained through a variety of data sources. The Pentobarbital Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Mebumal manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mebumal, including repackagers and relabelers. The FDA regulates Mebumal manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mebumal 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 Mebumal supplier is an individual or a company that provides Mebumal active pharmaceutical ingredient (API) or Mebumal finished formulations upon request. The Mebumal suppliers may include Mebumal API manufacturers, exporters, distributors and traders.
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A Mebumal CEP of the European Pharmacopoeia monograph is often referred to as a Mebumal Certificate of Suitability (COS). The purpose of a Mebumal CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Mebumal EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Mebumal to their clients by showing that a Mebumal CEP has been issued for it. The manufacturer submits a Mebumal CEP (COS) as part of the market authorization procedure, and it takes on the role of a Mebumal CEP holder for the record. Additionally, the data presented in the Mebumal CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Mebumal DMF.
A Mebumal CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Mebumal 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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