FDA NDC Directory · JSON-LD · Markdown

PROPAFENONE HYDROCHLORIDE

NDC 60687-930 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA075938
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsPROPAFENONE HYDROCHLORIDE (150 mg/1)
Marketing started20251021
Package count1

External sources

Source: openFDA. Public-domain (CC0).