01 2Chemische Fabrik Berg GmbH Bitterfeld-Wolfen DE
02 1AREVIPHARMA GMBH Radebeul DE
03 1EGIS Pharmaceuticals PLC Budapest HU
04 2EXCELLA GMBH & CO. KG Feucht DE
05 1OLON S.P.A. Rodano IT
06 1TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL
01 4Tamoxifen citrate
02 1Tamoxifen citrate, Micronised
03 1Tamoxifen citrate, Micronised, Non-micronised
04 1Tamoxifen citrate, Micronised, Non-micronised [10102/3]
05 1Tamoxifen citrate, Milled A; Milled Z
01 1Gabon
02 4Germany
03 1Hungary
04 1Israel
05 1Italy
01 6Valid
02 2Withdrawn by Holder
Tamoxifen Citrate, Micronised, Non-micronised [1...
Certificate Number : CEP 2022-463 - Rev 01
Status : Valid
Issue Date : 2024-09-27
Type : Chemical
Substance Number : 1046
Tamoxifen Citrate, Micronised, Non-micronised
Certificate Number : R1-CEP 2002-242 - Rev 05
Status : Valid
Issue Date : 2022-06-13
Type : Chemical
Substance Number : 1046
Certificate Number : R1-CEP 2005-197 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2013-05-17
Type : Chemical
Substance Number : 1046
Certificate Number : R1-CEP 1996-098 - Rev 09
Status : Valid
Issue Date : 2020-03-11
Type : Chemical
Substance Number : 1046
Certificate Number : R2-CEP 1995-016 - Rev 05
Status : Valid
Issue Date : 2020-08-20
Type : Chemical
Substance Number : 1046
Certificate Number : R1-CEP 1999-180 - Rev 06
Status : Valid
Issue Date : 2021-12-21
Type : Chemical
Substance Number : 1046
Tamoxifen Citrate, Milled A; Milled Z
Certificate Number : CEP 2021-495 - Rev 02
Status : Valid
Issue Date : 2024-10-28
Type : Chemical
Substance Number : 1046
Certificate Number : R1-CEP 1996-076 - Rev 05
Status : Withdrawn by Holder
Issue Date : 2014-06-06
Type : Chemical
Substance Number : 1046
A Tamoxifen Citrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tamoxifen Citrate, including repackagers and relabelers. The FDA regulates Tamoxifen Citrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tamoxifen Citrate 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 Tamoxifen Citrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tamoxifen Citrate supplier is an individual or a company that provides Tamoxifen Citrate active pharmaceutical ingredient (API) or Tamoxifen Citrate finished formulations upon request. The Tamoxifen Citrate suppliers may include Tamoxifen Citrate API manufacturers, exporters, distributors and traders.
click here to find a list of Tamoxifen Citrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tamoxifen Citrate CEP of the European Pharmacopoeia monograph is often referred to as a Tamoxifen Citrate Certificate of Suitability (COS). The purpose of a Tamoxifen Citrate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Tamoxifen Citrate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Tamoxifen Citrate to their clients by showing that a Tamoxifen Citrate CEP has been issued for it. The manufacturer submits a Tamoxifen Citrate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Tamoxifen Citrate CEP holder for the record. Additionally, the data presented in the Tamoxifen Citrate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Tamoxifen Citrate DMF.
A Tamoxifen Citrate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Tamoxifen Citrate 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 Tamoxifen Citrate suppliers with CEP (COS) on PharmaCompass.
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