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 1GlaxoSmithKline Research & Development Limited London GB
07 1LUSOCHIMICA S.P.A. Lomagna IT
08 2MELODY HEALTHCARE PVT. LTD. Mumbai IN
09 1OLON S.P.A. Rodano IT
10 1TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL
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.
Certificate Number : R1-CEP 2000-143 - Rev 07
Status : Valid
Issue Date : 2022-03-15
Type : Chemical
Substance Number : 687
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PharmaCompass offers a list of Salbutamol Sulphate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Salbutamol Sulphate manufacturer or Salbutamol Sulphate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Salbutamol Sulphate manufacturer or Salbutamol Sulphate supplier.
PharmaCompass also assists you with knowing the Salbutamol Sulphate API Price utilized in the formulation of products. Salbutamol Sulphate API Price is not always fixed or binding as the Salbutamol Sulphate Price is obtained through a variety of data sources. The Salbutamol Sulphate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A DUONEB manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DUONEB, including repackagers and relabelers. The FDA regulates DUONEB manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DUONEB 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 DUONEB manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A DUONEB supplier is an individual or a company that provides DUONEB active pharmaceutical ingredient (API) or DUONEB finished formulations upon request. The DUONEB suppliers may include DUONEB API manufacturers, exporters, distributors and traders.
click here to find a list of DUONEB suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A DUONEB CEP of the European Pharmacopoeia monograph is often referred to as a DUONEB Certificate of Suitability (COS). The purpose of a DUONEB CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of DUONEB EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of DUONEB to their clients by showing that a DUONEB CEP has been issued for it. The manufacturer submits a DUONEB CEP (COS) as part of the market authorization procedure, and it takes on the role of a DUONEB CEP holder for the record. Additionally, the data presented in the DUONEB CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the DUONEB DMF.
A DUONEB CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. DUONEB 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 DUONEB suppliers with CEP (COS) on PharmaCompass.
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