01 1Chemische Fabrik Berg GmbH Bitterfeld-Wolfen DE
02 1RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA S.P.A. Milano IT
03 1SHANGHAI WONDER PHARMACEUTICAL CO., LTD Shanghai CN
01 3Dimenhydrinate
01 1China
02 1Germany
03 1Italy
01 3Valid
Certificate Number : R1-CEP 2000-235 - Rev 05
Status : Valid
Issue Date : 2022-01-13
Type : Chemical
Substance Number : 601
Certificate Number : CEP 2017-283 - Rev 01
Status : Valid
Issue Date : 2024-01-19
Type : Chemical
Substance Number : 601
Certificate Number : CEP 2020-110 - Rev 01
Status : Valid
Issue Date : 2024-02-15
Type : Chemical
Substance Number : 601
81
PharmaCompass offers a list of Dimenhydrinate 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 Dimenhydrinate manufacturer or Dimenhydrinate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dimenhydrinate manufacturer or Dimenhydrinate supplier.
PharmaCompass also assists you with knowing the Dimenhydrinate API Price utilized in the formulation of products. Dimenhydrinate API Price is not always fixed or binding as the Dimenhydrinate Price is obtained through a variety of data sources. The Dimenhydrinate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Vomex A manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vomex A, including repackagers and relabelers. The FDA regulates Vomex A manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vomex A 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 Vomex A supplier is an individual or a company that provides Vomex A active pharmaceutical ingredient (API) or Vomex A finished formulations upon request. The Vomex A suppliers may include Vomex A API manufacturers, exporters, distributors and traders.
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A Vomex A CEP of the European Pharmacopoeia monograph is often referred to as a Vomex A Certificate of Suitability (COS). The purpose of a Vomex A CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Vomex A EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Vomex A to their clients by showing that a Vomex A CEP has been issued for it. The manufacturer submits a Vomex A CEP (COS) as part of the market authorization procedure, and it takes on the role of a Vomex A CEP holder for the record. Additionally, the data presented in the Vomex A CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Vomex A DMF.
A Vomex A CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Vomex A 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 Vomex A suppliers with CEP (COS) on PharmaCompass.
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