01 1CADILA PHARMACEUTICALS LIMITED Ankleshwar IN
02 1HETERO DRUGS LIMITED Hyderabad IN
03 1JIANGSU WEIQIDA PHARMACEUTICAL CO., LTD. Nantong City CN
04 1LUSOCHIMICA S.P.A. Casaletto Lodigiano IT
05 1MSN PHARMACHEM PRIVATE LIMITED Sangareddy District IN
06 1TORRENT PHARMACEUTICALS LIMITED Ahmedabad IN
07 1ZHEJIANG AUSUN PHARMACEUTICAL CO., LTD. Taizhou CN
08 1ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD. Linhai CN
01 7Nebivolol hydrochloride
02 1Nebivolol hydrochloride, Crystalline
01 3China
02 4India
03 1Italy
01 8Valid
Certificate Number : R0-CEP 2022-095 - Rev 00
Status : Valid
Issue Date : 2022-08-31
Type : Chemical
Substance Number : 2775
Certificate Number : CEP 2021-403 - Rev 01
Status : Valid
Issue Date : 2024-12-03
Type : Chemical
Substance Number : 2775
Certificate Number : CEP 2023-063 - Rev 01
Status : Valid
Issue Date : 2024-07-30
Type : Chemical
Substance Number : 2775
Nebivolol Hydrochloride, Crystalline
Certificate Number : CEP 2022-193 - Rev 01
Status : Valid
Issue Date : 2024-03-13
Type : Chemical
Substance Number : 2775
Certificate Number : CEP 2022-069 - Rev 00
Status : Valid
Issue Date : 2024-04-25
Type : Chemical
Substance Number : 2775
Certificate Number : CEP 2023-122 - Rev 00
Status : Valid
Issue Date : 2024-07-19
Type : Chemical
Substance Number : 2775
Certificate Number : R0-CEP 2022-170 - Rev 00
Status : Valid
Issue Date : 2022-12-09
Type : Chemical
Substance Number : 2775
Certificate Number : CEP 2022-140 - Rev 01
Status : Valid
Issue Date : 2023-12-20
Type : Chemical
Substance Number : 2775
A Nebivolol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nebivolol, including repackagers and relabelers. The FDA regulates Nebivolol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nebivolol 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 Nebivolol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Nebivolol supplier is an individual or a company that provides Nebivolol active pharmaceutical ingredient (API) or Nebivolol finished formulations upon request. The Nebivolol suppliers may include Nebivolol API manufacturers, exporters, distributors and traders.
click here to find a list of Nebivolol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Nebivolol CEP of the European Pharmacopoeia monograph is often referred to as a Nebivolol Certificate of Suitability (COS). The purpose of a Nebivolol CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Nebivolol EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Nebivolol to their clients by showing that a Nebivolol CEP has been issued for it. The manufacturer submits a Nebivolol CEP (COS) as part of the market authorization procedure, and it takes on the role of a Nebivolol CEP holder for the record. Additionally, the data presented in the Nebivolol CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Nebivolol DMF.
A Nebivolol CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Nebivolol 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 Nebivolol suppliers with CEP (COS) on PharmaCompass.
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