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01 1Mitsubishi Tanabe Pharma
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01 1DL-TRYPTOPHAN
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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 : 1317
Submission : 1969-01-23
Status : Inactive
Type : II
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PharmaCompass also assists you with knowing the Dl-Tryptophan API Price utilized in the formulation of products. Dl-Tryptophan API Price is not always fixed or binding as the Dl-Tryptophan Price is obtained through a variety of data sources. The Dl-Tryptophan Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A AM20060836 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AM20060836, including repackagers and relabelers. The FDA regulates AM20060836 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AM20060836 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 AM20060836 supplier is an individual or a company that provides AM20060836 active pharmaceutical ingredient (API) or AM20060836 finished formulations upon request. The AM20060836 suppliers may include AM20060836 API manufacturers, exporters, distributors and traders.
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A AM20060836 DMF (Drug Master File) is a document detailing the whole manufacturing process of AM20060836 active pharmaceutical ingredient (API) in detail. Different forms of AM20060836 DMFs exist exist since differing nations have different regulations, such as AM20060836 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A AM20060836 DMF submitted to regulatory agencies in the US is known as a USDMF. AM20060836 USDMF includes data on AM20060836's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The AM20060836 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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