01 1SIGMA TAU
01 1QUINACRINE HCL.
01 1U.S.A
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3905
Submission : 1980-08-08
Status : Inactive
Type : II
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PharmaCompass offers a list of Quinacrine 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 Quinacrine manufacturer or Quinacrine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Quinacrine manufacturer or Quinacrine supplier.
PharmaCompass also assists you with knowing the Quinacrine API Price utilized in the formulation of products. Quinacrine API Price is not always fixed or binding as the Quinacrine Price is obtained through a variety of data sources. The Quinacrine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Atabrine hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Atabrine hydrochloride, including repackagers and relabelers. The FDA regulates Atabrine hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Atabrine 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 Atabrine hydrochloride supplier is an individual or a company that provides Atabrine hydrochloride active pharmaceutical ingredient (API) or Atabrine hydrochloride finished formulations upon request. The Atabrine hydrochloride suppliers may include Atabrine hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Atabrine hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Atabrine hydrochloride DMF (Drug Master File) is a document detailing the whole manufacturing process of Atabrine hydrochloride active pharmaceutical ingredient (API) in detail. Different forms of Atabrine hydrochloride DMFs exist exist since differing nations have different regulations, such as Atabrine hydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Atabrine hydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. Atabrine hydrochloride USDMF includes data on Atabrine hydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Atabrine hydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
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