01 1DEVATS INDIA
01 1NIMORAZOLE
01 1India
01 1Active
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 24814
Submission : 2011-03-30
Status : Active
Type : II
A Nimorazole manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nimorazole, including repackagers and relabelers. The FDA regulates Nimorazole manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nimorazole 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 Nimorazole manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Nimorazole supplier is an individual or a company that provides Nimorazole active pharmaceutical ingredient (API) or Nimorazole finished formulations upon request. The Nimorazole suppliers may include Nimorazole API manufacturers, exporters, distributors and traders.
click here to find a list of Nimorazole suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Nimorazole DMF (Drug Master File) is a document detailing the whole manufacturing process of Nimorazole active pharmaceutical ingredient (API) in detail. Different forms of Nimorazole DMFs exist exist since differing nations have different regulations, such as Nimorazole USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Nimorazole DMF submitted to regulatory agencies in the US is known as a USDMF. Nimorazole USDMF includes data on Nimorazole's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Nimorazole USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Nimorazole suppliers with USDMF on PharmaCompass.
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