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01 1CETIEDIL
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01 1Inactive
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USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5011
Submission : 1983-08-01
Status : Inactive
Type : II
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A Cetiedil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cetiedil, including repackagers and relabelers. The FDA regulates Cetiedil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cetiedil 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 Cetiedil supplier is an individual or a company that provides Cetiedil active pharmaceutical ingredient (API) or Cetiedil finished formulations upon request. The Cetiedil suppliers may include Cetiedil API manufacturers, exporters, distributors and traders.
click here to find a list of Cetiedil suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cetiedil DMF (Drug Master File) is a document detailing the whole manufacturing process of Cetiedil active pharmaceutical ingredient (API) in detail. Different forms of Cetiedil DMFs exist exist since differing nations have different regulations, such as Cetiedil USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Cetiedil DMF submitted to regulatory agencies in the US is known as a USDMF. Cetiedil USDMF includes data on Cetiedil's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Cetiedil USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Cetiedil suppliers with USDMF on PharmaCompass.
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