01 1The Moleculez
01 1POVIDONE IODINE IP/BP/EP/USP
01 1India
01 1Active
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 43341
Submission : 2025-12-26
Status : Active
Type : II
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A Luviskol K90 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Luviskol K90, including repackagers and relabelers. The FDA regulates Luviskol K90 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Luviskol K90 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 Luviskol K90 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Luviskol K90 supplier is an individual or a company that provides Luviskol K90 active pharmaceutical ingredient (API) or Luviskol K90 finished formulations upon request. The Luviskol K90 suppliers may include Luviskol K90 API manufacturers, exporters, distributors and traders.
click here to find a list of Luviskol K90 suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Luviskol K90 DMF (Drug Master File) is a document detailing the whole manufacturing process of Luviskol K90 active pharmaceutical ingredient (API) in detail. Different forms of Luviskol K90 DMFs exist exist since differing nations have different regulations, such as Luviskol K90 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Luviskol K90 DMF submitted to regulatory agencies in the US is known as a USDMF. Luviskol K90 USDMF includes data on Luviskol K90's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Luviskol K90 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Luviskol K90 suppliers with USDMF on PharmaCompass.
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