FDA NDC Directory · JSON-LD · Markdown

Imiquimod

NDC 87519-004 · HUMAN PRESCRIPTION DRUG · CREAM

Labeler / ManufacturerAnvi Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA205971
Dosage form / routeCREAM · TOPICAL
Active ingredientsIMIQUIMOD (37.5 mg/g)
Marketing started20260901
Package count1

External sources

Source: openFDA. Public-domain (CC0).