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