01 1Muby Chem
01 1SODIUM HYPOCHLORITE SOLUTION USP
01 1India
01 1Active
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 43069
Submission : 2026-02-02
Status : Active
Type : IV
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A Clorox manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Clorox, including repackagers and relabelers. The FDA regulates Clorox manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Clorox 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 Clorox manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Clorox supplier is an individual or a company that provides Clorox active pharmaceutical ingredient (API) or Clorox finished formulations upon request. The Clorox suppliers may include Clorox API manufacturers, exporters, distributors and traders.
click here to find a list of Clorox suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Clorox DMF (Drug Master File) is a document detailing the whole manufacturing process of Clorox active pharmaceutical ingredient (API) in detail. Different forms of Clorox DMFs exist exist since differing nations have different regulations, such as Clorox USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Clorox DMF submitted to regulatory agencies in the US is known as a USDMF. Clorox USDMF includes data on Clorox's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Clorox USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Clorox suppliers with USDMF on PharmaCompass.
