FDA NDC Directory · JSON-LD · Markdown

FAMOTIDINE

NDC 72205-233 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SUSPENSION

Labeler / ManufacturerNovadoz Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA219863
Dosage form / routePOWDER, FOR SUSPENSION · ORAL
Active ingredientsFAMOTIDINE (40 mg/5mL)
Marketing started20250724
Package count1

External sources

Source: openFDA. Public-domain (CC0).