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01 1HealthTech BioActives
01 1DIOSMETIN
01 1Spain
01 1Active
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 40274
Submission : 2024-08-14
Status : Active
Type : II
A Diosmetin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Diosmetin, including repackagers and relabelers. The FDA regulates Diosmetin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Diosmetin 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 Diosmetin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Diosmetin supplier is an individual or a company that provides Diosmetin active pharmaceutical ingredient (API) or Diosmetin finished formulations upon request. The Diosmetin suppliers may include Diosmetin API manufacturers, exporters, distributors and traders.
click here to find a list of Diosmetin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Diosmetin DMF (Drug Master File) is a document detailing the whole manufacturing process of Diosmetin active pharmaceutical ingredient (API) in detail. Different forms of Diosmetin DMFs exist exist since differing nations have different regulations, such as Diosmetin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Diosmetin DMF submitted to regulatory agencies in the US is known as a USDMF. Diosmetin USDMF includes data on Diosmetin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Diosmetin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Diosmetin suppliers with USDMF on PharmaCompass.
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