01 2APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
02 2CIPLA LIMITED Mumbai IN
03 2HETERO LABS LIMITED Hyderabad IN
04 1SHANGHAI DESANO CHEMICAL PHARMACEUTICAL CO., LTD. Laogang Town CN
05 1SUN PHARMACEUTICAL INDUSTRIES LIMITED Mumbai IN
06 1TIANISH LABORATORIES PRIVATE LIMITED Hyderabad IN
07 2ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD. Linhai CN
01 5Nevirapine
02 3Nevirapine hemihydrate
03 1Nevirapine, 017905
04 1Nevirapine, Additional site
05 1Nevirapine, Process II
01 3China
02 8India
01 7Valid
02 4Withdrawn by Holder
Certificate Number : CEP 2012-184 - Rev 02
Status : Valid
Issue Date : 2024-01-12
Type : Chemical
Substance Number : 2255
Certificate Number : CEP 2024-062 - Rev 00
Status : Valid
Issue Date : 2024-08-08
Type : Chemical
Substance Number : 2479
Certificate Number : R1-CEP 2013-079 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2018-09-10
Type : Chemical
Substance Number : 2479
Certificate Number : CEP 2016-076 - Rev 01
Status : Valid
Issue Date : 2024-07-18
Type : Chemical
Substance Number : 2255
Certificate Number : R1-CEP 2008-145 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2018-02-08
Type : Chemical
Substance Number : 2255
Certificate Number : R0-CEP 2020-267 - Rev 00
Status : Valid
Issue Date : 2022-12-12
Type : Chemical
Substance Number : 2255
Certificate Number : R1-CEP 2008-222 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2015-06-04
Type : Chemical
Substance Number : 2255
Certificate Number : CEP 2011-075 - Rev 05
Status : Valid
Issue Date : 2024-07-18
Type : Chemical
Substance Number : 2255
Certificate Number : R1-CEP 2016-153 - Rev 00
Status : Valid
Issue Date : 2023-01-19
Type : Chemical
Substance Number : 2479
Certificate Number : R1-CEP 2011-223 - Rev 01
Status : Valid
Issue Date : 2021-07-06
Type : Chemical
Substance Number : 2255
A Nevirapine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nevirapine, including repackagers and relabelers. The FDA regulates Nevirapine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nevirapine 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 Nevirapine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Nevirapine supplier is an individual or a company that provides Nevirapine active pharmaceutical ingredient (API) or Nevirapine finished formulations upon request. The Nevirapine suppliers may include Nevirapine API manufacturers, exporters, distributors and traders.
click here to find a list of Nevirapine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Nevirapine CEP of the European Pharmacopoeia monograph is often referred to as a Nevirapine Certificate of Suitability (COS). The purpose of a Nevirapine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Nevirapine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Nevirapine to their clients by showing that a Nevirapine CEP has been issued for it. The manufacturer submits a Nevirapine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Nevirapine CEP holder for the record. Additionally, the data presented in the Nevirapine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Nevirapine DMF.
A Nevirapine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Nevirapine 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 Nevirapine suppliers with CEP (COS) on PharmaCompass.
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