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01 1Takeda Pharmaceutical
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01 1BULK PRODUCTION OF OXENDOLONE IN THE HIKARI PLANT
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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 : 5609
Submission : 1984-10-24
Status : Inactive
Type : II
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PharmaCompass offers a list of Oxendolone 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 Oxendolone manufacturer or Oxendolone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Oxendolone manufacturer or Oxendolone supplier.
PharmaCompass also assists you with knowing the Oxendolone API Price utilized in the formulation of products. Oxendolone API Price is not always fixed or binding as the Oxendolone Price is obtained through a variety of data sources. The Oxendolone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A TSAA 291 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of TSAA 291, including repackagers and relabelers. The FDA regulates TSAA 291 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. TSAA 291 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 TSAA 291 supplier is an individual or a company that provides TSAA 291 active pharmaceutical ingredient (API) or TSAA 291 finished formulations upon request. The TSAA 291 suppliers may include TSAA 291 API manufacturers, exporters, distributors and traders.
click here to find a list of TSAA 291 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A TSAA 291 DMF (Drug Master File) is a document detailing the whole manufacturing process of TSAA 291 active pharmaceutical ingredient (API) in detail. Different forms of TSAA 291 DMFs exist exist since differing nations have different regulations, such as TSAA 291 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A TSAA 291 DMF submitted to regulatory agencies in the US is known as a USDMF. TSAA 291 USDMF includes data on TSAA 291's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The TSAA 291 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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