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01 Farmabios SpA Gropello Cairoli IT (1)
02 Hubei Gedian Humanwell Pharmaceutical Co., Ltd. E-Zhou CN (2)
03 BAYER AG Leverkusen DE (2)
04 CIPLA LIMITED Mumbai IN (1)
05 CURIA SPAIN S.A.U. Boecillo ES (1)
06 JIANGSU GRAND XIANLE PHARMACEUTICAL CO., LTD. Yancheng CN (1)
07 NEWCHEM S.p.A. Milano IT (1)
08 TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL (1)
09 ZHEJIANG XIANJU PHARMACEUTICAL CO., LTD. Xianju CN (2)
01 Cyproterone acetate (7)
02 Cyproterone acetate, Micronised (2)
03 Cyproterone acetate, Process A (1)
04 Cyproterone acetate, Process II (1)
05 Cyproterone acetate, Variant 1 (1)
01 China (5)
02 Germany (2)
03 India (1)
04 Israel (1)
05 Italy (2)
06 Spain (1)
01 Valid (11)
02 Withdrawn by Holder (1)
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PharmaCompass offers a list of Cyproterone Acetate 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 Cyproterone Acetate manufacturer or Cyproterone Acetate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cyproterone Acetate manufacturer or Cyproterone Acetate supplier.
PharmaCompass also assists you with knowing the Cyproterone Acetate API Price utilized in the formulation of products. Cyproterone Acetate API Price is not always fixed or binding as the Cyproterone Acetate Price is obtained through a variety of data sources. The Cyproterone Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A DSSTox_CID_366 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DSSTox_CID_366, including repackagers and relabelers. The FDA regulates DSSTox_CID_366 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DSSTox_CID_366 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of DSSTox_CID_366 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A DSSTox_CID_366 supplier is an individual or a company that provides DSSTox_CID_366 active pharmaceutical ingredient (API) or DSSTox_CID_366 finished formulations upon request. The DSSTox_CID_366 suppliers may include DSSTox_CID_366 API manufacturers, exporters, distributors and traders.
click here to find a list of DSSTox_CID_366 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A DSSTox_CID_366 CEP of the European Pharmacopoeia monograph is often referred to as a DSSTox_CID_366 Certificate of Suitability (COS). The purpose of a DSSTox_CID_366 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of DSSTox_CID_366 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of DSSTox_CID_366 to their clients by showing that a DSSTox_CID_366 CEP has been issued for it. The manufacturer submits a DSSTox_CID_366 CEP (COS) as part of the market authorization procedure, and it takes on the role of a DSSTox_CID_366 CEP holder for the record. Additionally, the data presented in the DSSTox_CID_366 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the DSSTox_CID_366 DMF.
A DSSTox_CID_366 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. DSSTox_CID_366 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 DSSTox_CID_366 suppliers with CEP (COS) on PharmaCompass.
We have 9 companies offering DSSTox_CID_366
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