Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
01 1GRANULES INDIA LIMITED Hyderabad IN
02 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
03 1CHROMO LABORATORIES INDIA PRIVATE LIMITED Pashamylaram IN
04 1HETERO LABS LIMITED Hyderabad IN
05 1MSN PHARMACHEM PRIVATE LIMITED Sangareddy District IN
06 1SHANGHAI DESANO CHEMICAL PHARMACEUTICAL CO., LTD. Laogang Town CN
07 1TIANISH LABORATORIES PRIVATE LIMITED Hyderabad IN
01 7Atazanavir sulfate
01 1China
02 6India
01 7Valid
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
Certificate Number : CEP 2020-279 - Rev 01
Status : Valid
Issue Date : 2024-06-10
Type : Chemical
Substance Number : 2898
Certificate Number : CEP 2020-031 - Rev 01
Status : Valid
Issue Date : 2023-12-06
Type : Chemical
Substance Number : 2898
Certificate Number : R0-CEP 2019-177 - Rev 00
Status : Valid
Issue Date : 2022-09-21
Type : Chemical
Substance Number : 2898
Certificate Number : CEP 2019-217 - Rev 01
Status : Valid
Issue Date : 2024-09-11
Type : Chemical
Substance Number : 2898
Certificate Number : CEP 2019-331 - Rev 01
Status : Valid
Issue Date : 2023-10-24
Type : Chemical
Substance Number : 2898
Certificate Number : R0-CEP 2021-115 - Rev 00
Status : Valid
Issue Date : 2023-08-25
Type : Chemical
Substance Number : 2898
Certificate Number : CEP 2019-203 - Rev 03
Status : Valid
Issue Date : 2024-07-24
Type : Chemical
Substance Number : 2898
A Atazanavir Sulfate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Atazanavir Sulfate, including repackagers and relabelers. The FDA regulates Atazanavir Sulfate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Atazanavir Sulfate 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 Atazanavir Sulfate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Atazanavir Sulfate supplier is an individual or a company that provides Atazanavir Sulfate active pharmaceutical ingredient (API) or Atazanavir Sulfate finished formulations upon request. The Atazanavir Sulfate suppliers may include Atazanavir Sulfate API manufacturers, exporters, distributors and traders.
click here to find a list of Atazanavir Sulfate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Atazanavir Sulfate CEP of the European Pharmacopoeia monograph is often referred to as a Atazanavir Sulfate Certificate of Suitability (COS). The purpose of a Atazanavir Sulfate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Atazanavir Sulfate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Atazanavir Sulfate to their clients by showing that a Atazanavir Sulfate CEP has been issued for it. The manufacturer submits a Atazanavir Sulfate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Atazanavir Sulfate CEP holder for the record. Additionally, the data presented in the Atazanavir Sulfate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Atazanavir Sulfate DMF.
A Atazanavir Sulfate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Atazanavir Sulfate 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 Atazanavir Sulfate suppliers with CEP (COS) on PharmaCompass.
We have 7 companies offering Atazanavir Sulfate
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