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01 2Chemische Fabrik Berg GmbH Bitterfeld-Wolfen DE
02 1AREVIPHARMA GMBH Radebeul DE
03 1EXCELLA GMBH & CO. KG Feucht DE
04 1OLON S.P.A. Rodano IT
05 1TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL
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01 3Tamoxifen citrate
02 1Tamoxifen citrate, Micronised
03 1Tamoxifen citrate, Micronised, Non-micronised
04 1Tamoxifen citrate, Micronised, Non-micronised [10102/3]
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01 4Germany
02 1Israel
03 1Italy
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01 5Valid
02 1Withdrawn by Holder
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
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
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Status : Withdrawn by Holder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
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PharmaCompass offers a list of Tamoxifen Citrate 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 Tamoxifen Citrate manufacturer or Tamoxifen Citrate supplier for your needs.
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A Tox21_300274 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_300274, including repackagers and relabelers. The FDA regulates Tox21_300274 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_300274 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 Tox21_300274 supplier is an individual or a company that provides Tox21_300274 active pharmaceutical ingredient (API) or Tox21_300274 finished formulations upon request. The Tox21_300274 suppliers may include Tox21_300274 API manufacturers, exporters, distributors and traders.
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A Tox21_300274 CEP of the European Pharmacopoeia monograph is often referred to as a Tox21_300274 Certificate of Suitability (COS). The purpose of a Tox21_300274 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Tox21_300274 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Tox21_300274 to their clients by showing that a Tox21_300274 CEP has been issued for it. The manufacturer submits a Tox21_300274 CEP (COS) as part of the market authorization procedure, and it takes on the role of a Tox21_300274 CEP holder for the record. Additionally, the data presented in the Tox21_300274 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Tox21_300274 DMF.
A Tox21_300274 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Tox21_300274 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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We have 5 companies offering Tox21_300274
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