Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.
01 2EGIS Pharmaceuticals PLC Budapest HU
02 1EUROAPI GERMANY GmbH Frankfurt am Main DE
03 2AARTI PHARMALABS LIMITED Mulund (W), Mumbai IN
04 1NEULAND LABORATORIES LIMITED Hyderabad IN
05 1Farmhispania, S.A. Montmeló ES
06 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
07 1ARCH PHARMALABS LIMITED Mumbai IN
08 1CIPLA LIMITED Mumbai IN
09 1DR. REDDY'S LABORATORIES LIMITED Hyderabad IN
10 1ESTEVE QUIMICA S.A. Barcelona ES
11 2HETERO LABS LIMITED Hyderabad IN
12 1LUPIN LIMITED Mumbai IN
13 1MELODY HEALTHCARE PVT. LTD. Boisar IN
14 1SMS PHARMACEUTICALS LIMITED Hyderabad IN
15 1SUN PHARMACEUTICAL INDUSTRIES LIMITED Mumbai IN
16 1UNIMARK REMEDIES LIMITED Mumbai IN
17 2ZHEJIANG CHANGMING PHARMACEUTICAL CO., LTD. Tiantai CN
18 1ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD. Linhai CN
Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.
Certificate Number : R0-CEP 2020-284 - Rev 01
Status : Valid
Issue Date : 2023-02-28
Type : Chemical
Substance Number : 1368
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Certificate Number : R1-CEP 2001-297 - Rev 07
Status : Valid
Issue Date : 2021-12-10
Type : Chemical
Substance Number : 1368
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Certificate Number : R1-CEP 2006-040 - Rev 06
Status : Valid
Issue Date : 2022-10-14
Type : Chemical
Substance Number : 1368
Neuland Laboratories- A dedicated 100% API provider.
Certificate Number : R1-CEP 2003-219 - Rev 07
Status : Valid
Issue Date : 2022-12-16
Type : Chemical
Substance Number : 1368
Farmhispania Group, a leading European CDMO in HPAPI Technologies & High Potency Fermentation.
Certificate Number : R1-CEP 2004-224 - Rev 02
Status : Valid
Issue Date : 2019-10-17
Type : Chemical
Substance Number : 1368
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Certificate Number : R1-CEP 2009-083 - Rev 05
Status : Valid
Issue Date : 2022-10-14
Type : Chemical
Substance Number : 1368
A Ramipril manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ramipril, including repackagers and relabelers. The FDA regulates Ramipril manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ramipril 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 Ramipril manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ramipril supplier is an individual or a company that provides Ramipril active pharmaceutical ingredient (API) or Ramipril finished formulations upon request. The Ramipril suppliers may include Ramipril API manufacturers, exporters, distributors and traders.
click here to find a list of Ramipril suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Ramipril CEP of the European Pharmacopoeia monograph is often referred to as a Ramipril Certificate of Suitability (COS). The purpose of a Ramipril CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Ramipril EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Ramipril to their clients by showing that a Ramipril CEP has been issued for it. The manufacturer submits a Ramipril CEP (COS) as part of the market authorization procedure, and it takes on the role of a Ramipril CEP holder for the record. Additionally, the data presented in the Ramipril CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Ramipril DMF.
A Ramipril CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Ramipril 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 Ramipril suppliers with CEP (COS) on PharmaCompass.
We have 17 companies offering Ramipril
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