Expand your portfolio with Egis- value-added generics, API capabilities, and reliable contract services to drive your growth.

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01 1EGIS 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 1EGIS PHARMACEUTICALS PLC. Budapest X HU
09 1F Hoffmann-La Roche Ltd. Basel CH
10 1IPCA Laboratories Limited Mumbai IN
11 1KRKA, d.d., Novo mesto Novo mesto SI
12 1LUPIN LIMITED Mumbai IN
13 1QILU PHARMACEUTICAL CO., LTD. Jinan CN
14 1SHODHANA LABORATORIES PRIVATE LIMITED Hyderabad IN
15 1SUN PHARMACEUTICAL INDUSTRIES LIMITED Mumbai IN
16 1SYMED LABS LIMITED Hyderabad IN
17 1TIANISH LABORATORIES PRIVATE LIMITED Hyderabad IN
18 1URQUIMA S.A. Sant Fost De Campsentelles ES
19 1ZAKLADY FARMACEUTYCZNE POLPHARMA S.A. Starogard Gdanski PL
20 1ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD. Linhai CN
21 1ZYDUS LIFESCIENCES LIMITED Vadodara IN
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01 18Carvedilol
02 1Carvedilol, Micronised
03 1Carvedilol, Process-II, micronised
04 1Carvedilol, Site-II
05 1Carvedilol, Synthetic route B
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01 2China
02 1Germany
03 1Hungary
04 13India
05 1Slovenia
06 1Spain
07 1U.S.A
08 2Blank
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01 17Valid
02 5Withdrawn by Holder
Expand your portfolio with Egis- value-added generics, API capabilities, and reliable contract services to drive your growth.
Expand your portfolio with Egis- value-added generics, API capabilities, and reliable contract services to drive your growth.
Certificate Number : R1-CEP 2003-042 - Rev 03
Status : Valid
Issue Date : 2019-02-20
Type : Chemical
Substance Number : 1745
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Certificate Number : CEP 2006-136 - Rev 06
Status : Valid
Issue Date : 2023-11-17
Type : Chemical
Substance Number : 1745

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Carvedilol, Process-II, Micronised
Certificate Number : CEP 2024-534 - Rev 00
Status : Valid
Issue Date : 2025-02-28
Type : Chemical
Substance Number : 1745

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Certificate Number : R1-CEP 2005-124 - Rev 03
Status : Valid
Issue Date : 2018-03-09
Type : Chemical
Substance Number : 1745

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Certificate Number : CEP 2014-201 - Rev 02
Status : Valid
Issue Date : 2025-01-20
Type : Chemical
Substance Number : 1745

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Certificate Number : R1-CEP 2002-001 - Rev 03
Status : Valid
Issue Date : 2012-07-25
Type : Chemical
Substance Number : 1745

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Certificate Number : R1-CEP 2008-259 - Rev 01
Status : Valid
Issue Date : 2022-07-28
Type : Chemical
Substance Number : 1745

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Certificate Number : R1-CEP 2004-230 - Rev 05
Status : Valid
Issue Date : 2015-07-28
Type : Chemical
Substance Number : 1745

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Certificate Number : R0-CEP 2021-109 - Rev 00
Status : Valid
Issue Date : 2023-05-17
Type : Chemical
Substance Number : 1745

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Certificate Number : CEP 2016-314 - Rev 01
Status : Valid
Issue Date : 2026-04-10
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, and more, enabling you to easily find the right Carvedilol manufacturer or Carvedilol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Carvedilol manufacturer or Carvedilol supplier.
A carvedilol hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of carvedilol hydrochloride, including repackagers and relabelers. The FDA regulates carvedilol hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. carvedilol hydrochloride 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 carvedilol hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A carvedilol hydrochloride supplier is an individual or a company that provides carvedilol hydrochloride active pharmaceutical ingredient (API) or carvedilol hydrochloride finished formulations upon request. The carvedilol hydrochloride suppliers may include carvedilol hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of carvedilol hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A carvedilol hydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a carvedilol hydrochloride Certificate of Suitability (COS). The purpose of a carvedilol hydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of carvedilol hydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of carvedilol hydrochloride to their clients by showing that a carvedilol hydrochloride CEP has been issued for it. The manufacturer submits a carvedilol hydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a carvedilol hydrochloride CEP holder for the record. Additionally, the data presented in the carvedilol hydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the carvedilol hydrochloride DMF.
A carvedilol hydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. carvedilol hydrochloride 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 carvedilol hydrochloride suppliers with CEP (COS) on PharmaCompass.
We have 18 companies offering carvedilol hydrochloride
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