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Imiquimod

NDC 68462-536 · HUMAN PRESCRIPTION DRUG · CREAM

Labeler / ManufacturerGlenmark Pharmaceuticals Inc., USA
Marketing categoryAbbreviated NDA (generic) · App ANDA201994
Dosage form / routeCREAM · TOPICAL
Active ingredientsIMIQUIMOD (50 mg/g)
Marketing started20120306
Package count1

External sources

Source: openFDA. Public-domain (CC0).