01 1Rhodia Organique SAS
01 1ETHOPROPAZINE
01 1France
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 536
Submission : 1963-04-12
Status : Inactive
Type : II
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PharmaCompass offers a list of Profenamine 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 Profenamine manufacturer or Profenamine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Profenamine manufacturer or Profenamine supplier.
PharmaCompass also assists you with knowing the Profenamine API Price utilized in the formulation of products. Profenamine API Price is not always fixed or binding as the Profenamine Price is obtained through a variety of data sources. The Profenamine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Parsidol hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Parsidol hydrochloride, including repackagers and relabelers. The FDA regulates Parsidol hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Parsidol hydrochloride API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Parsidol hydrochloride supplier is an individual or a company that provides Parsidol hydrochloride active pharmaceutical ingredient (API) or Parsidol hydrochloride finished formulations upon request. The Parsidol hydrochloride suppliers may include Parsidol hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Parsidol hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Parsidol hydrochloride DMF (Drug Master File) is a document detailing the whole manufacturing process of Parsidol hydrochloride active pharmaceutical ingredient (API) in detail. Different forms of Parsidol hydrochloride DMFs exist exist since differing nations have different regulations, such as Parsidol hydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Parsidol hydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. Parsidol hydrochloride USDMF includes data on Parsidol hydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Parsidol hydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Parsidol hydrochloride suppliers with USDMF on PharmaCompass.
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