01 1Mitsubishi Tanabe Pharma
01 1DL - METHIONINE
01 1Japan
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 1832
Submission : 1971-12-17
Status : Inactive
Type : II
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PharmaCompass offers a list of Methionine 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 Methionine manufacturer or Methionine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Methionine manufacturer or Methionine supplier.
PharmaCompass also assists you with knowing the Methionine API Price utilized in the formulation of products. Methionine API Price is not always fixed or binding as the Methionine Price is obtained through a variety of data sources. The Methionine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 0XD manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 0XD, including repackagers and relabelers. The FDA regulates 0XD manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 0XD 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 0XD manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 0XD supplier is an individual or a company that provides 0XD active pharmaceutical ingredient (API) or 0XD finished formulations upon request. The 0XD suppliers may include 0XD API manufacturers, exporters, distributors and traders.
click here to find a list of 0XD suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A 0XD DMF (Drug Master File) is a document detailing the whole manufacturing process of 0XD active pharmaceutical ingredient (API) in detail. Different forms of 0XD DMFs exist exist since differing nations have different regulations, such as 0XD USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A 0XD DMF submitted to regulatory agencies in the US is known as a USDMF. 0XD USDMF includes data on 0XD's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 0XD USDMF is kept confidential to protect the manufacturer’s intellectual property.
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