01 1Proto Chemical Industries
01 1IODOFORM USP
01 1India
01 1Active
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 32097
Submission : 2017-09-21
Status : Active
Type : II
A Iodoform manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Iodoform, including repackagers and relabelers. The FDA regulates Iodoform manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Iodoform 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 Iodoform manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Iodoform supplier is an individual or a company that provides Iodoform active pharmaceutical ingredient (API) or Iodoform finished formulations upon request. The Iodoform suppliers may include Iodoform API manufacturers, exporters, distributors and traders.
click here to find a list of Iodoform suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Iodoform DMF (Drug Master File) is a document detailing the whole manufacturing process of Iodoform active pharmaceutical ingredient (API) in detail. Different forms of Iodoform DMFs exist exist since differing nations have different regulations, such as Iodoform USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Iodoform DMF submitted to regulatory agencies in the US is known as a USDMF. Iodoform USDMF includes data on Iodoform's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Iodoform USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Iodoform suppliers with USDMF on PharmaCompass.
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