01 1XINJIANG NUZILINE BIO-PHARMACEUTICAL CO., LTD. Tuergen CN
01 1Estrogens, conjugated, 3.00% in lactose monohydrate
01 1China
01 1Valid
Estrogens, Conjugated, 3.00% In Lactose Monohydr...
Certificate Number : R1-CEP 2010-153 - Rev 00
Status : Valid
Issue Date : 2018-02-19
Type : Chemical
Substance Number : 1512
92
PharmaCompass offers a list of Conjugated Estrogens 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 Conjugated Estrogens manufacturer or Conjugated Estrogens supplier for your needs.
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PharmaCompass also assists you with knowing the Conjugated Estrogens API Price utilized in the formulation of products. Conjugated Estrogens API Price is not always fixed or binding as the Conjugated Estrogens Price is obtained through a variety of data sources. The Conjugated Estrogens Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Premarin Vaginal manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Premarin Vaginal, including repackagers and relabelers. The FDA regulates Premarin Vaginal manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Premarin Vaginal 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 Premarin Vaginal supplier is an individual or a company that provides Premarin Vaginal active pharmaceutical ingredient (API) or Premarin Vaginal finished formulations upon request. The Premarin Vaginal suppliers may include Premarin Vaginal API manufacturers, exporters, distributors and traders.
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A Premarin Vaginal CEP of the European Pharmacopoeia monograph is often referred to as a Premarin Vaginal Certificate of Suitability (COS). The purpose of a Premarin Vaginal CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Premarin Vaginal EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Premarin Vaginal to their clients by showing that a Premarin Vaginal CEP has been issued for it. The manufacturer submits a Premarin Vaginal CEP (COS) as part of the market authorization procedure, and it takes on the role of a Premarin Vaginal CEP holder for the record. Additionally, the data presented in the Premarin Vaginal CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Premarin Vaginal DMF.
A Premarin Vaginal CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Premarin Vaginal 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 Premarin Vaginal suppliers with CEP (COS) on PharmaCompass.
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