Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
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01 1AARTI PHARMALABS LIMITED Mulund (W), Mumbai IN
02 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
03 2APOTEX PHARMACHEM INDIA PVT. LTD Bangalore IN
04 1ARCH PHARMALABS LIMITED Mumbai IN
05 1BACHEM S.A. Vionnaz CH
06 1GLENMARK LIFE SCIENCES LIMITED Mumbai IN
07 1HETERO DRUGS LIMITED Hyderabad IN
08 1IPCA LABORATORIES LIMITED Mumbai IN
09 2KRKA, d.d., Novo mesto Novo mesto SI
10 1LUPIN LIMITED Mumbai IN
11 1Laboratorios Servier S.L. Toledo ES
12 1NINGBO MENOVO PHARMACEUTICAL CO., LTD. Ningbo Hi-Tech District CN
13 1ORIL INDUSTRIE Bolbec FR
14 1PIRAMAL PHARMA LIMITED Hyderabad IN
15 1ROLABO OUTSOURCING, S.L. Zaragoza ES
16 1TIANISH LABORATORIES PRIVATE LIMITED Hyderabad IN
17 1ZHEJIANG CHANGMING PHARMACEUTICAL CO., LTD. Tiantai CN
18 2ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD. Linhai CN
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01 16Perindopril tert-butylamine
02 1Perindopril tert-butylamine, Code 301644
03 1Perindopril tert-butylamine, Code 302281
04 1Perindopril tert-butylamine, Laboratorios Servier S.L. (Spain, Toledo)
05 1Perindopril tert-butylamine, PER55LP
06 1Perindopril tert-butylamine, Process 2
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01 2Canada
02 4China
03 2France
04 8India
05 2Slovenia
06 1Spain
07 1Switzerland
08 1U.S.A
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01 18Valid
02 3Withdrawn by Holder
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Certificate Number : R1-CEP 2013-245 - Rev 02
Status : Valid
Issue Date : 2022-10-27
Type : Chemical
Substance Number : 2019
Perindopril Tert-butylamine, PER55LP
Certificate Number : CEP 2019-196 - Rev 02
Status : Valid
Issue Date : 2024-12-23
Type : Chemical
Substance Number : 2019
Certificate Number : R1-CEP 2004-279 - Rev 05
Status : Valid
Issue Date : 2022-12-05
Type : Chemical
Substance Number : 2019
Certificate Number : R1-CEP 2010-118 - Rev 04
Status : Valid
Issue Date : 2021-07-27
Type : Chemical
Substance Number : 2019
Perindopril Tert-butylamine, Code 301644
Certificate Number : R0-CEP 2019-245 - Rev 01
Status : Valid
Issue Date : 2022-03-07
Type : Chemical
Substance Number : 2019
Certificate Number : CEP 2022-207 - Rev 00
Status : Valid
Issue Date : 2024-02-28
Type : Chemical
Substance Number : 2019
Certificate Number : CEP 2004-284 - Rev 02
Status : Valid
Issue Date : 2024-01-11
Type : Chemical
Substance Number : 2019
Certificate Number : CEP 2010-157 - Rev 05
Status : Valid
Issue Date : 2024-08-08
Type : Chemical
Substance Number : 2019
Certificate Number : CEP 2023-355 - Rev 00
Status : Valid
Issue Date : 2025-01-21
Type : Chemical
Substance Number : 2019
Perindopril Tert-butylamine, Process 2
Certificate Number : R0-CEP 2020-356 - Rev 00
Status : Valid
Issue Date : 2021-02-24
Type : Chemical
Substance Number : 2019
75
PharmaCompass offers a list of Perindopril Erbumine 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 Perindopril Erbumine manufacturer or Perindopril Erbumine supplier for your needs.
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A Perindopril Erbumine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Perindopril Erbumine, including repackagers and relabelers. The FDA regulates Perindopril Erbumine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Perindopril Erbumine 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 Perindopril Erbumine supplier is an individual or a company that provides Perindopril Erbumine active pharmaceutical ingredient (API) or Perindopril Erbumine finished formulations upon request. The Perindopril Erbumine suppliers may include Perindopril Erbumine API manufacturers, exporters, distributors and traders.
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A Perindopril Erbumine CEP of the European Pharmacopoeia monograph is often referred to as a Perindopril Erbumine Certificate of Suitability (COS). The purpose of a Perindopril Erbumine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Perindopril Erbumine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Perindopril Erbumine to their clients by showing that a Perindopril Erbumine CEP has been issued for it. The manufacturer submits a Perindopril Erbumine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Perindopril Erbumine CEP holder for the record. Additionally, the data presented in the Perindopril Erbumine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Perindopril Erbumine DMF.
A Perindopril Erbumine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Perindopril Erbumine 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 16 companies offering Perindopril Erbumine
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