01 1Fujifilm Diosynth Biotechnologies
01 1METHANDRIOL
01 1United Kingdom
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4619
Submission : 1982-08-02
Status : Inactive
Type : II
A Methandriol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Methandriol, including repackagers and relabelers. The FDA regulates Methandriol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Methandriol 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 Methandriol supplier is an individual or a company that provides Methandriol active pharmaceutical ingredient (API) or Methandriol finished formulations upon request. The Methandriol suppliers may include Methandriol API manufacturers, exporters, distributors and traders.
click here to find a list of Methandriol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Methandriol DMF (Drug Master File) is a document detailing the whole manufacturing process of Methandriol active pharmaceutical ingredient (API) in detail. Different forms of Methandriol DMFs exist exist since differing nations have different regulations, such as Methandriol USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Methandriol DMF submitted to regulatory agencies in the US is known as a USDMF. Methandriol USDMF includes data on Methandriol's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Methandriol USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Methandriol suppliers with USDMF on PharmaCompass.
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