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
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01 1Brompheniramine maleate
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01 1India
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01 1Valid
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 : R1-CEP 2015-097 - Rev 00
Status : Valid
Issue Date : 2023-01-19
Type : Chemical
Substance Number : 977
79
PharmaCompass offers a list of Brompheniramine Maleate 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 Brompheniramine Maleate manufacturer or Brompheniramine Maleate supplier for your needs.
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PharmaCompass also assists you with knowing the Brompheniramine Maleate API Price utilized in the formulation of products. Brompheniramine Maleate API Price is not always fixed or binding as the Brompheniramine Maleate Price is obtained through a variety of data sources. The Brompheniramine Maleate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Dimotane manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dimotane, including repackagers and relabelers. The FDA regulates Dimotane manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dimotane 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 Dimotane manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dimotane supplier is an individual or a company that provides Dimotane active pharmaceutical ingredient (API) or Dimotane finished formulations upon request. The Dimotane suppliers may include Dimotane API manufacturers, exporters, distributors and traders.
click here to find a list of Dimotane suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Dimotane CEP of the European Pharmacopoeia monograph is often referred to as a Dimotane Certificate of Suitability (COS). The purpose of a Dimotane CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Dimotane EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Dimotane to their clients by showing that a Dimotane CEP has been issued for it. The manufacturer submits a Dimotane CEP (COS) as part of the market authorization procedure, and it takes on the role of a Dimotane CEP holder for the record. Additionally, the data presented in the Dimotane CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Dimotane DMF.
A Dimotane CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Dimotane 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 Dimotane suppliers with CEP (COS) on PharmaCompass.
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