Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
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01 1SUPRIYA LIFESCIENCE LTD. Mumbai IN
02 1Boehringer Ingelheim Pharma GmbH & Co. KG Ingelheim Am Rhein DE
03 3CIPLA LIMITED Mumbai IN
04 1FDC Limited Mumbai IN
05 1GlaxoSmithKline Research & Development Limited London GB
06 1LUSOCHIMICA S.P.A. Lomagna IT
07 1MELODY HEALTHCARE PRIVATE LIMITED Mumbai IN
08 1MELODY HEALTHCARE PVT. LTD. Mumbai IN
09 1OLON S.P.A. Rodano IT
10 1TAPI NL B.V. Amsterdam NL
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01 9Salbutamol sulfate
02 1Salbutamol sulfate, Code 6885
03 1Salbutamol sulfate, Micronised
04 1Salbutamol sulfate, Process III, Non-micronised and Micronised
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01 1Germany
02 7India
03 2Italy
04 1United Kingdom
05 1Blank
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01 12Valid
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Certificate Number : CEP 2019-037 - Rev 01
Status : Valid
Issue Date : 2024-09-25
Type : Chemical
Substance Number : 687
Certificate Number : CEP 1997-004 - Rev 05
Status : Valid
Issue Date : 2024-05-30
Type : Chemical
Substance Number : 687
Certificate Number : CEP 2005-080 - Rev 06
Status : Valid
Issue Date : 2024-03-07
Type : Chemical
Substance Number : 687
Certificate Number : CEP 2011-314 - Rev 03
Status : Valid
Issue Date : 2024-03-07
Type : Chemical
Substance Number : 687
Certificate Number : CEP 2015-212 - Rev 02
Status : Valid
Issue Date : 2024-06-12
Type : Chemical
Substance Number : 687
Certificate Number : CEP 2023-371 - Rev 00
Status : Valid
Issue Date : 2025-03-20
Type : Chemical
Substance Number : 687
Certificate Number : CEP 2005-235 - Rev 03
Status : Valid
Issue Date : 2024-04-02
Type : Chemical
Substance Number : 687
Salbutamol Sulfate, Micronised
Certificate Number : CEP 2020-063 - Rev 03
Status : Valid
Issue Date : 2025-09-22
Type : Chemical
Substance Number : 687
Certificate Number : CEP 2014-193 - Rev 01
Status : Valid
Issue Date : 2024-03-18
Type : Chemical
Substance Number : 687
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Certificate Number : CEP 2020-100 - Rev 03
Status : Valid
Issue Date : 2025-07-04
Type : Chemical
Substance Number : 687
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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A PROAIR RESPICLICK manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of PROAIR RESPICLICK, including repackagers and relabelers. The FDA regulates PROAIR RESPICLICK manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. PROAIR RESPICLICK API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A PROAIR RESPICLICK supplier is an individual or a company that provides PROAIR RESPICLICK active pharmaceutical ingredient (API) or PROAIR RESPICLICK finished formulations upon request. The PROAIR RESPICLICK suppliers may include PROAIR RESPICLICK API manufacturers, exporters, distributors and traders.
click here to find a list of PROAIR RESPICLICK suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A PROAIR RESPICLICK CEP of the European Pharmacopoeia monograph is often referred to as a PROAIR RESPICLICK Certificate of Suitability (COS). The purpose of a PROAIR RESPICLICK CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of PROAIR RESPICLICK EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of PROAIR RESPICLICK to their clients by showing that a PROAIR RESPICLICK CEP has been issued for it. The manufacturer submits a PROAIR RESPICLICK CEP (COS) as part of the market authorization procedure, and it takes on the role of a PROAIR RESPICLICK CEP holder for the record. Additionally, the data presented in the PROAIR RESPICLICK CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the PROAIR RESPICLICK DMF.
A PROAIR RESPICLICK CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. PROAIR RESPICLICK CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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