Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
01 1PHARMACEUTICAL WORKS POLPHARMA S.A. Starogard Gdanski PL
02 2EGIS Pharmaceuticals PLC Budapest HU
03 1Moehs Iberica S.L. Rubi ES
04 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
05 1AREVIPHARMA GMBH Radebeul DE
06 1AUROBINDO PHARMA LIMITED Hyderabad IN
07 1CADILA PHARMACEUTICALS LIMITED Ankleshwar IN
08 1CIPLA LIMITED Mumbai IN
09 1CTX LIFESCIENCES PVT. LIMITED Surat IN
10 1DR. REDDY'S LABORATORIES LIMITED Hyderabad IN
11 1F Hoffmann-La Roche Ltd. Basel CH
12 1IPCA Laboratories Limited Mumbai IN
13 1KRKA, d.d., Novo mesto Novo mesto SI
14 1LUPIN LIMITED Mumbai IN
15 1PHARMAZELL (INDIA) PRIVATE LIMITED Chennai IN
16 1QILU PHARMACEUTICAL CO., LTD. Jinan CN
17 1SHODHANA LABORATORIES PRIVATE LIMITED Hyderabad IN
18 1SUN PHARMACEUTICAL INDUSTRIES LIMITED Mumbai IN
19 1SYMED LABS LIMITED Hyderabad IN
20 1TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL
21 1TIANISH LABORATORIES PRIVATE LIMITED Hyderabad IN
22 1URQUIMA S.A. Sant Fost De Campsentelles ES
23 1USV Limited Mumbai IN
24 1ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD. Linhai CN
25 1ZYDUS LIFESCIENCES LIMITED Vadodara IN
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
Certificate Number : R1-CEP 2002-258 - Rev 08
Status : Valid
Issue Date : 2021-10-22
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
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Certificate Number : R1-CEP 2002-089 - Rev 03
Status : Valid
Issue Date : 2019-02-28
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 2003-042 - Rev 03
Status : Valid
Issue Date : 2019-02-20
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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Carvedilol manufacturer or Carvedilol supplier.
PharmaCompass also assists you with knowing the Carvedilol API Price utilized in the formulation of products. Carvedilol API Price is not always fixed or binding as the Carvedilol Price is obtained through a variety of data sources. The Carvedilol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
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.
click here to find a list of Carvedilol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
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.
click here to find a list of Carvedilol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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.
click here to find a list of Carvedilol suppliers with CEP (COS) on PharmaCompass.
We have 21 companies offering Carvedilol
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