01 1AbbVie Inc. North Chicago US
02 1ANHUI BIOCHEM PHARMACEUTICAL CO., LTD. Fuyang CN
03 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
04 1ARENE LIFE SCIENCES PRIVATE LIMITED Sangareddy IN
05 1CHROMO LABORATORIES INDIA PRIVATE LIMITED Pashamylaram IN
06 1HETERO DRUGS LIMITED Hyderabad IN
07 1LAURUS LABS LIMITED Hyderabad IN
08 1MYLAN LABORATORIES LIMITED Hyderabad IN
09 2SHANGHAI DESANO CHEMICAL PHARMACEUTICAL CO., LTD. Laogang Town CN
10 2TIANISH LABORATORIES PRIVATE LIMITED Hyderabad IN
01 7Ritonavir
02 2Ritonavir, Form-I
03 1Ritonavir, Form-I, RII process
04 2Ritonavir, Form-II
01 3China
02 7India
03 2U.S.A
01 11Valid
02 1Withdrawn by Holder
Certificate Number : R1-CEP 2012-397 - Rev 00
Status : Valid
Issue Date : 2019-09-19
Type : Chemical
Substance Number : 2136
Certificate Number : CEP 2022-394 - Rev 00
Status : Valid
Issue Date : 2024-12-17
Type : Chemical
Substance Number : 2136
Certificate Number : CEP 2022-293 - Rev 00
Status : Valid
Issue Date : 2024-01-03
Type : Chemical
Substance Number : 2136
Certificate Number : CEP 2018-061 - Rev 02
Status : Valid
Issue Date : 2024-10-08
Type : Chemical
Substance Number : 2136
Certificate Number : CEP 2020-235 - Rev 01
Status : Valid
Issue Date : 2024-12-13
Type : Chemical
Substance Number : 2136
Certificate Number : R0-CEP 2020-102 - Rev 01
Status : Valid
Issue Date : 2023-03-28
Type : Chemical
Substance Number : 2136
Certificate Number : R0-CEP 2020-416 - Rev 00
Status : Valid
Issue Date : 2021-05-12
Type : Chemical
Substance Number : 2136
Certificate Number : CEP 2017-229 - Rev 03
Status : Valid
Issue Date : 2024-09-03
Type : Chemical
Substance Number : 2136
Certificate Number : CEP 2011-221 - Rev 02
Status : Valid
Issue Date : 2024-07-25
Type : Chemical
Substance Number : 2136
Certificate Number : CEP 2011-346 - Rev 01
Status : Valid
Issue Date : 2024-07-25
Type : Chemical
Substance Number : 2136
A Ritonavir manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ritonavir, including repackagers and relabelers. The FDA regulates Ritonavir manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ritonavir 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 Ritonavir manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ritonavir supplier is an individual or a company that provides Ritonavir active pharmaceutical ingredient (API) or Ritonavir finished formulations upon request. The Ritonavir suppliers may include Ritonavir API manufacturers, exporters, distributors and traders.
click here to find a list of Ritonavir suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Ritonavir CEP of the European Pharmacopoeia monograph is often referred to as a Ritonavir Certificate of Suitability (COS). The purpose of a Ritonavir CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Ritonavir EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Ritonavir to their clients by showing that a Ritonavir CEP has been issued for it. The manufacturer submits a Ritonavir CEP (COS) as part of the market authorization procedure, and it takes on the role of a Ritonavir CEP holder for the record. Additionally, the data presented in the Ritonavir CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Ritonavir DMF.
A Ritonavir CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Ritonavir 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 Ritonavir suppliers with CEP (COS) on PharmaCompass.
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