EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1EUROAPI GERMANY GmbH Frankfurt am Main DE
02 1AARTI PHARMALABS LIMITED Mulund (W), Mumbai IN
03 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
04 1ARCH PHARMALABS LIMITED Mumbai IN
05 1CIPLA LIMITED Mumbai IN
06 1ESTEVE QUIMICA S.A. Barcelona ES
07 1Farmhispania, S.A. Montmeló ES
08 2HETERO LABS LIMITED Hyderabad IN
09 1LUPIN LIMITED Mumbai IN
10 1MELODY HEALTHCARE PVT. LTD. Boisar IN
11 1SMS PHARMACEUTICALS LIMITED Hyderabad IN
12 1SUN PHARMACEUTICAL INDUSTRIES LIMITED Mumbai IN
13 2ZHEJIANG CHANGMING PHARMACEUTICAL CO., LTD. Taizhou CN
14 1ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD. Linhai CN
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 pharmaceutical companies for APIs & Intermediates. Largest Indian producer of Caffeine.
Certificate Number : R1-CEP 2006-040 - Rev 06
Status : Valid
Issue Date : 2022-10-14
Type : Chemical
Substance Number : 1368
96
PharmaCompass offers a list of Ramipril 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 Ramipril manufacturer or Ramipril supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ramipril manufacturer or Ramipril supplier.
PharmaCompass also assists you with knowing the Ramipril API Price utilized in the formulation of products. Ramipril API Price is not always fixed or binding as the Ramipril Price is obtained through a variety of data sources. The Ramipril Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Altace manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Altace, including repackagers and relabelers. The FDA regulates Altace manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Altace 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 Altace manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Altace supplier is an individual or a company that provides Altace active pharmaceutical ingredient (API) or Altace finished formulations upon request. The Altace suppliers may include Altace API manufacturers, exporters, distributors and traders.
click here to find a list of Altace suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Altace CEP of the European Pharmacopoeia monograph is often referred to as a Altace Certificate of Suitability (COS). The purpose of a Altace CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Altace EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Altace to their clients by showing that a Altace CEP has been issued for it. The manufacturer submits a Altace CEP (COS) as part of the market authorization procedure, and it takes on the role of a Altace CEP holder for the record. Additionally, the data presented in the Altace CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Altace DMF.
A Altace CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Altace 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 Altace suppliers with CEP (COS) on PharmaCompass.
We have 14 companies offering Altace
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