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Serving leading biopharmaceutical companies globally:

Johnson and Johnson
Express Scripts
Federal Trade Commission

Generated: February 23, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 006882

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NDA 006882 describes PHISOHEX, which is a drug marketed by Sanofi Aventis Us and is included in two NDAs. Additional details are available on the PHISOHEX profile page.

The generic ingredient in PHISOHEX is hexachlorophene. There are seven drug master file entries for this compound. Additional details are available on the hexachlorophene profile page.
Summary for 006882
Applicant:Sanofi Aventis Us
Formulation / Manufacturing:see details
Pharmacology for NDA: 006882
Medical Subject Heading (MeSH) Categories for 006882

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:EMULSION;TOPICALStrength3%
Approval Date:Approved Prior to Jan 1, 1982TE:RLD:No

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Serving hundreds of leading biopharmaceutical companies globally:

Queensland Health
US Army
Federal Trade Commission
Chinese Patent Office
Argus Health

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