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 2APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
03 1AREVIPHARMA GMBH Radebeul DE
04 1AUROBINDO PHARMA LIMITED Hyderabad IN
05 1CADILA PHARMACEUTICALS LIMITED Ankleshwar IN
06 1CIPLA LIMITED Mumbai IN
07 1CTX LIFESCIENCES PVT. LIMITED Surat IN
08 1F Hoffmann-La Roche Ltd. Basel CH
09 1IPCA Laboratories Limited Mumbai IN
10 1KRKA, d.d., Novo mesto Novo mesto SI
11 1LUPIN LIMITED Mumbai IN
12 1QILU PHARMACEUTICAL CO., LTD. Jinan CN
13 1SHODHANA LABORATORIES PRIVATE LIMITED Hyderabad IN
14 1SUN PHARMACEUTICAL INDUSTRIES LIMITED Mumbai IN
15 1SYMED LABS LIMITED Hyderabad IN
16 1TIANISH LABORATORIES PRIVATE LIMITED Hyderabad IN
17 1URQUIMA S.A. Sant Fost De Campsentelles ES
18 1ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD. Linhai CN
19 1ZYDUS LIFESCIENCES LIMITED Vadodara IN
Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.
Certificate Number : R1-CEP 2003-042 - Rev 03
Status : Valid
Issue Date : 2019-02-20
Type : Chemical
Substance Number : 1745
Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.
Certificate Number : R1-CEP 2016-314 - Rev 00
Status : Valid
Issue Date : 2023-08-28
Type : Chemical
Substance Number : 1745
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PharmaCompass offers a list of Carvedilol 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 Carvedilol manufacturer or Carvedilol supplier for your needs.
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A Carvedilol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Carvedilol, including repackagers and relabelers. The FDA regulates Carvedilol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Carvedilol 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 Carvedilol supplier is an individual or a company that provides Carvedilol active pharmaceutical ingredient (API) or Carvedilol finished formulations upon request. The Carvedilol suppliers may include Carvedilol API manufacturers, exporters, distributors and traders.
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A Carvedilol CEP of the European Pharmacopoeia monograph is often referred to as a Carvedilol Certificate of Suitability (COS). The purpose of a Carvedilol CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Carvedilol EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Carvedilol to their clients by showing that a Carvedilol CEP has been issued for it. The manufacturer submits a Carvedilol CEP (COS) as part of the market authorization procedure, and it takes on the role of a Carvedilol CEP holder for the record. Additionally, the data presented in the Carvedilol CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Carvedilol DMF.
A Carvedilol CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Carvedilol 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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