01 1Daiichi Sankyo
02 1Nihon Nohyaku
01 1MALOTILATE
02 1MALOTILATE 200 MG TABLETS
01 2Japan
01 2Inactive
01 2Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5347
Submission : 1984-05-03
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5356
Submission : 1984-05-03
Status : Inactive
Type : II
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PharmaCompass offers a list of MALOTILATE 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 MALOTILATE manufacturer or MALOTILATE supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred MALOTILATE manufacturer or MALOTILATE supplier.
PharmaCompass also assists you with knowing the MALOTILATE API Price utilized in the formulation of products. MALOTILATE API Price is not always fixed or binding as the MALOTILATE Price is obtained through a variety of data sources. The MALOTILATE Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A DA-3857 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DA-3857, including repackagers and relabelers. The FDA regulates DA-3857 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DA-3857 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 DA-3857 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A DA-3857 supplier is an individual or a company that provides DA-3857 active pharmaceutical ingredient (API) or DA-3857 finished formulations upon request. The DA-3857 suppliers may include DA-3857 API manufacturers, exporters, distributors and traders.
click here to find a list of DA-3857 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A DA-3857 DMF (Drug Master File) is a document detailing the whole manufacturing process of DA-3857 active pharmaceutical ingredient (API) in detail. Different forms of DA-3857 DMFs exist exist since differing nations have different regulations, such as DA-3857 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A DA-3857 DMF submitted to regulatory agencies in the US is known as a USDMF. DA-3857 USDMF includes data on DA-3857's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The DA-3857 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of DA-3857 suppliers with USDMF on PharmaCompass.
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