Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
01 1SUPRIYA LIFESCIENCE LTD. Mumbai IN
02 1NEULAND LABORATORIES LIMITED Hyderabad IN
03 1Boehringer Ingelheim Pharma GmbH & Co. KG Ingelheim Am Rhein DE
04 2CIPLA LIMITED Mumbai IN
05 1FDC Limited Mumbai IN
06 1LUSOCHIMICA S.P.A. Lomagna IT
07 2MELODY HEALTHCARE PVT. LTD. Mumbai IN
08 1OLON S.P.A. Rodano IT
09 1TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL
01 9Salbutamol sulfate
02 1Salbutamol sulfate, Code 6885
03 1Salbutamol sulfate, Micronised
01 1Germany
02 7India
03 1Israel
04 2Italy
01 11Valid
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
Neuland Laboratories- A dedicated 100% API provider.
Neuland Laboratories- A dedicated 100% API provider.
Certificate Number : R1-CEP 2000-143 - Rev 07
Status : Valid
Issue Date : 2022-03-15
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 2014-193 - Rev 01
Status : Valid
Issue Date : 2024-03-18
Type : Chemical
Substance Number : 687
Salbutamol Sulfate, Micronised
Certificate Number : CEP 2020-063 - Rev 02
Status : Valid
Issue Date : 2024-03-25
Type : Chemical
Substance Number : 687
Certificate Number : CEP 2021-191 - Rev 01
Status : Valid
Issue Date : 2024-02-06
Type : Chemical
Substance Number : 687
Certificate Number : CEP 2020-100 - Rev 02
Status : Valid
Issue Date : 2024-10-24
Type : Chemical
Substance Number : 687
A Fartolin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fartolin, including repackagers and relabelers. The FDA regulates Fartolin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fartolin 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 Fartolin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fartolin supplier is an individual or a company that provides Fartolin active pharmaceutical ingredient (API) or Fartolin finished formulations upon request. The Fartolin suppliers may include Fartolin API manufacturers, exporters, distributors and traders.
click here to find a list of Fartolin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Fartolin CEP of the European Pharmacopoeia monograph is often referred to as a Fartolin Certificate of Suitability (COS). The purpose of a Fartolin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Fartolin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Fartolin to their clients by showing that a Fartolin CEP has been issued for it. The manufacturer submits a Fartolin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Fartolin CEP holder for the record. Additionally, the data presented in the Fartolin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Fartolin DMF.
A Fartolin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Fartolin 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 Fartolin suppliers with CEP (COS) on PharmaCompass.
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