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01 1SAFC
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01 1ETHYLENE OXIDE STERILISATION
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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 : 17262
Submission : 2004-03-26
Status : Inactive
Type : II
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PharmaCompass offers a list of Homotaurine 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 Homotaurine manufacturer or Homotaurine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Homotaurine manufacturer or Homotaurine supplier.
PharmaCompass also assists you with knowing the Homotaurine API Price utilized in the formulation of products. Homotaurine API Price is not always fixed or binding as the Homotaurine Price is obtained through a variety of data sources. The Homotaurine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 3-APS manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 3-APS, including repackagers and relabelers. The FDA regulates 3-APS manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 3-APS 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 3-APS manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 3-APS supplier is an individual or a company that provides 3-APS active pharmaceutical ingredient (API) or 3-APS finished formulations upon request. The 3-APS suppliers may include 3-APS API manufacturers, exporters, distributors and traders.
click here to find a list of 3-APS suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A 3-APS DMF (Drug Master File) is a document detailing the whole manufacturing process of 3-APS active pharmaceutical ingredient (API) in detail. Different forms of 3-APS DMFs exist exist since differing nations have different regulations, such as 3-APS USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A 3-APS DMF submitted to regulatory agencies in the US is known as a USDMF. 3-APS USDMF includes data on 3-APS's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 3-APS USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of 3-APS suppliers with USDMF on PharmaCompass.