Cosma S.p.A.: FDA-approved API manufacturing with 300+ tons capacity, serving pharma and animal health industries worldwide.
01 1Cosma
02 2Amoli Organics
03 1Assertio Therapeutics
04 2J.B.Chemicals & Pharmaceuticals
05 1YUNG ZIP CHEMICAL INDUSTRIAL
Cosma S.p.A.: FDA-approved API manufacturing with 300+ tons capacity, serving pharma and animal health industries worldwide.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 27322
Submission : 2014-03-04
Status :
Type : II
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PharmaCompass offers a list of Diclofenac 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 Diclofenac manufacturer or Diclofenac supplier for your needs.
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PharmaCompass also assists you with knowing the Diclofenac API Price utilized in the formulation of products. Diclofenac API Price is not always fixed or binding as the Diclofenac Price is obtained through a variety of data sources. The Diclofenac Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Voltaren SR manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Voltaren SR, including repackagers and relabelers. The FDA regulates Voltaren SR manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Voltaren SR 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 Voltaren SR supplier is an individual or a company that provides Voltaren SR active pharmaceutical ingredient (API) or Voltaren SR finished formulations upon request. The Voltaren SR suppliers may include Voltaren SR API manufacturers, exporters, distributors and traders.
click here to find a list of Voltaren SR suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Voltaren SR DMF (Drug Master File) is a document detailing the whole manufacturing process of Voltaren SR active pharmaceutical ingredient (API) in detail. Different forms of Voltaren SR DMFs exist exist since differing nations have different regulations, such as Voltaren SR USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Voltaren SR DMF submitted to regulatory agencies in the US is known as a USDMF. Voltaren SR USDMF includes data on Voltaren SR's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Voltaren SR USDMF is kept confidential to protect the manufacturer’s intellectual property.
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