01 1ALEMBIC LIMITED Vadodara IN
02 1Artemis Biotech Limited Hyderabad IN
03 2BIOCON LIMITED Bangalore IN
04 1CONCORD BIOTECH LIMITED Ahmedabad IN
05 1Henan Topfond Pharmaceutical Co., Ltd. Zhumadian CN
06 1KREBS BIOCHEMICALS & INDUSTRIES LIMITED Kothapalli IN
07 1KRKA, d.d., Novo mesto Novo mesto SI
08 1LEK PHARMACEUTICALS D.D. Ljubljana SI
09 1STERLING BIOTECH LIMITED Masar Village IN
10 1TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL
11 1Zhejiang Hisun Pharmaceutical Co., Ltd. Taizhou City CN
01 12Lovastatin
01 2China
02 7India
03 1Israel
04 2Slovenia
01 5Valid
02 7Withdrawn by Holder
Certificate Number : R0-CEP 2014-083 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2015-11-13
Type : Chemical
Substance Number : 1538
Certificate Number : R0-CEP 2003-269 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2006-08-03
Type : Chemical
Substance Number : 1538
Certificate Number : R0-CEP 2001-354 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2004-10-11
Type : Chemical
Substance Number : 1538
Certificate Number : R1-CEP 2004-115 - Rev 03
Status : Valid
Issue Date : 2021-05-17
Type : Chemical
Substance Number : 1538
Certificate Number : R0-CEP 2006-161 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2011-11-08
Type : Chemical
Substance Number : 1538
Certificate Number : R1-CEP 2004-026 - Rev 03
Status : Valid
Issue Date : 2023-08-04
Type : Chemical
Substance Number : 1538
Certificate Number : R1-CEP 2004-191 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2010-12-02
Type : Chemical
Substance Number : 1538
Certificate Number : R1-CEP 2014-146 - Rev 00
Status : Valid
Issue Date : 2020-03-16
Type : Chemical
Substance Number : 1538
Certificate Number : R1-CEP 2000-406 - Rev 05
Status : Valid
Issue Date : 2021-11-23
Type : Chemical
Substance Number : 1538
Certificate Number : R1-CEP 2001-406 - Rev 05
Status : Valid
Issue Date : 2021-07-02
Type : Chemical
Substance Number : 1538
17
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A Tox21_300268 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_300268, including repackagers and relabelers. The FDA regulates Tox21_300268 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_300268 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_300268 supplier is an individual or a company that provides Tox21_300268 active pharmaceutical ingredient (API) or Tox21_300268 finished formulations upon request. The Tox21_300268 suppliers may include Tox21_300268 API manufacturers, exporters, distributors and traders.
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A Tox21_300268 CEP of the European Pharmacopoeia monograph is often referred to as a Tox21_300268 Certificate of Suitability (COS). The purpose of a Tox21_300268 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Tox21_300268 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Tox21_300268 to their clients by showing that a Tox21_300268 CEP has been issued for it. The manufacturer submits a Tox21_300268 CEP (COS) as part of the market authorization procedure, and it takes on the role of a Tox21_300268 CEP holder for the record. Additionally, the data presented in the Tox21_300268 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Tox21_300268 DMF.
A Tox21_300268 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Tox21_300268 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 11 companies offering Tox21_300268
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