FDA NDC Directory · JSON-LD · Markdown

Podofilox

NDC 0574-0621 · HUMAN PRESCRIPTION DRUG · GEL

Labeler / ManufacturerPadagis US LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA211871
Dosage form / routeGEL · TOPICAL
Active ingredientsPODOFILOX (5 mg/g)
Marketing started20231213
Package count1

External sources

Source: openFDA. Public-domain (CC0).