01 PHARMACEUTICAL WORKS POLPHARMA S.A. Starogard Gdanski PL (2)
02 AMOLI ORGANICS PRIVATE LIMITED Mumbai IN (2)
03 AREVIPHARMA GMBH Radebeul DE (1)
04 Bajaj Healthcare Limited Mumbai IN (1)
05 CTX LIFESCIENCES PVT. LIMITED Surat IN (1)
06 Degussa AG Düsseldorf DE (1)
07 F.I.S. - FABBRICA ITALIANA SINTETICI S.P.A. Montecchio Maggiore IT (1)
08 Farchemia S.r.l. Treviglio IT (1)
09 JUBILANT PHARMOVA LIMITED Nanjangud IN (2)
10 PharmaZell GmbH Raubling DE (1)
11 SIEGFRIED EVIONNAZ SA Evionnaz CH (1)
12 TEVA PHARMACEUTICAL INDUSTRIES LTD Petach Tikva IL (1)
13 TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL (1)
14 ZHEJIANG RAYBOW PHARMACEUTICAL CO., LTD. Taizhou City CN (1)
15 Zhejiang Jiuzhou Pharmaceutical Co., Ltd. Taizhou City CN (1)
01 Carbamazepine (13)
02 Carbamazepine, CMZ (1)
03 Carbamazepine, Crystallised in ethanol (1)
04 Carbamazepine, Crystallization from ethanol (1)
05 Carbamazepine, Process B (1)
06 Carbamazepine, Process II (1)
01 China (1)
02 Germany (3)
03 India (6)
04 Israel (2)
05 Italy (2)
06 Poland (2)
07 Switzerland (1)
08 U.S.A (1)
01 Valid (13)
02 Withdrawn by EDQM Failure to CEP procedure (1)
03 Withdrawn by Holder (4)
79
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A Tox21_300195 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_300195, including repackagers and relabelers. The FDA regulates Tox21_300195 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_300195 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_300195 supplier is an individual or a company that provides Tox21_300195 active pharmaceutical ingredient (API) or Tox21_300195 finished formulations upon request. The Tox21_300195 suppliers may include Tox21_300195 API manufacturers, exporters, distributors and traders.
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A Tox21_300195 CEP of the European Pharmacopoeia monograph is often referred to as a Tox21_300195 Certificate of Suitability (COS). The purpose of a Tox21_300195 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Tox21_300195 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Tox21_300195 to their clients by showing that a Tox21_300195 CEP has been issued for it. The manufacturer submits a Tox21_300195 CEP (COS) as part of the market authorization procedure, and it takes on the role of a Tox21_300195 CEP holder for the record. Additionally, the data presented in the Tox21_300195 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Tox21_300195 DMF.
A Tox21_300195 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Tox21_300195 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 13 companies offering Tox21_300195
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