01 1EXPANSIA
01 1CICLETANINE
01 1France
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7508
Submission : 1988-06-01
Status : Inactive
Type : II
A Cicletanine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cicletanine, including repackagers and relabelers. The FDA regulates Cicletanine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cicletanine 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 Cicletanine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cicletanine supplier is an individual or a company that provides Cicletanine active pharmaceutical ingredient (API) or Cicletanine finished formulations upon request. The Cicletanine suppliers may include Cicletanine API manufacturers, exporters, distributors and traders.
click here to find a list of Cicletanine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cicletanine DMF (Drug Master File) is a document detailing the whole manufacturing process of Cicletanine active pharmaceutical ingredient (API) in detail. Different forms of Cicletanine DMFs exist exist since differing nations have different regulations, such as Cicletanine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Cicletanine DMF submitted to regulatory agencies in the US is known as a USDMF. Cicletanine USDMF includes data on Cicletanine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Cicletanine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Cicletanine suppliers with USDMF on PharmaCompass.
LOOKING FOR A SUPPLIER?