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01 1Pfizer Inc
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01 1N-ACETYLPROCAINAMIDE HCL.
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01 1U.S.A
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01 1Inactive
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01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6186
Submission : 1986-01-29
Status : Inactive
Type : II
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PharmaCompass offers a list of Acecainide 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 Acecainide manufacturer or Acecainide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Acecainide manufacturer or Acecainide supplier.
PharmaCompass also assists you with knowing the Acecainide API Price utilized in the formulation of products. Acecainide API Price is not always fixed or binding as the Acecainide Price is obtained through a variety of data sources. The Acecainide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A NAPA hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of NAPA hydrochloride, including repackagers and relabelers. The FDA regulates NAPA hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. NAPA 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 NAPA hydrochloride supplier is an individual or a company that provides NAPA hydrochloride active pharmaceutical ingredient (API) or NAPA hydrochloride finished formulations upon request. The NAPA hydrochloride suppliers may include NAPA hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of NAPA hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A NAPA hydrochloride DMF (Drug Master File) is a document detailing the whole manufacturing process of NAPA hydrochloride active pharmaceutical ingredient (API) in detail. Different forms of NAPA hydrochloride DMFs exist exist since differing nations have different regulations, such as NAPA hydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A NAPA hydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. NAPA hydrochloride USDMF includes data on NAPA hydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The NAPA hydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of NAPA hydrochloride suppliers with USDMF on PharmaCompass.
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