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01 1Taiho Pharmaceutical
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01 1GTS-21
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01 1Japan
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01 1Inactive
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01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 14645
Submission : 1999-12-28
Status : Inactive
Type : II
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PharmaCompass offers a list of 3-2,4-Dimethoxybenzylidene-Anabaseine 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 3-2,4-Dimethoxybenzylidene-Anabaseine manufacturer or 3-2,4-Dimethoxybenzylidene-Anabaseine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred 3-2,4-Dimethoxybenzylidene-Anabaseine manufacturer or 3-2,4-Dimethoxybenzylidene-Anabaseine supplier.
PharmaCompass also assists you with knowing the 3-2,4-Dimethoxybenzylidene-Anabaseine API Price utilized in the formulation of products. 3-2,4-Dimethoxybenzylidene-Anabaseine API Price is not always fixed or binding as the 3-2,4-Dimethoxybenzylidene-Anabaseine Price is obtained through a variety of data sources. The 3-2,4-Dimethoxybenzylidene-Anabaseine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A GTS 21 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of GTS 21, including repackagers and relabelers. The FDA regulates GTS 21 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. GTS 21 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 GTS 21 supplier is an individual or a company that provides GTS 21 active pharmaceutical ingredient (API) or GTS 21 finished formulations upon request. The GTS 21 suppliers may include GTS 21 API manufacturers, exporters, distributors and traders.
click here to find a list of GTS 21 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A GTS 21 DMF (Drug Master File) is a document detailing the whole manufacturing process of GTS 21 active pharmaceutical ingredient (API) in detail. Different forms of GTS 21 DMFs exist exist since differing nations have different regulations, such as GTS 21 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A GTS 21 DMF submitted to regulatory agencies in the US is known as a USDMF. GTS 21 USDMF includes data on GTS 21's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The GTS 21 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of GTS 21 suppliers with USDMF on PharmaCompass.
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