01 1Recordati
01 1FENTICONAZOLE NITRATE
01 1Italy
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7864
Submission : 1989-01-13
Status : Inactive
Type : II
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A Lomexin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lomexin, including repackagers and relabelers. The FDA regulates Lomexin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lomexin 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 Lomexin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Lomexin supplier is an individual or a company that provides Lomexin active pharmaceutical ingredient (API) or Lomexin finished formulations upon request. The Lomexin suppliers may include Lomexin API manufacturers, exporters, distributors and traders.
click here to find a list of Lomexin suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Lomexin DMF (Drug Master File) is a document detailing the whole manufacturing process of Lomexin active pharmaceutical ingredient (API) in detail. Different forms of Lomexin DMFs exist exist since differing nations have different regulations, such as Lomexin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Lomexin DMF submitted to regulatory agencies in the US is known as a USDMF. Lomexin USDMF includes data on Lomexin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Lomexin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Lomexin suppliers with USDMF on PharmaCompass.
