FDA NDC Directory · JSON-LD · Markdown

Famotidine

NDC 43598-572 · HUMAN PRESCRIPTION DRUG · FOR SUSPENSION

Labeler / ManufacturerDR. REDDY'S LABORATORIES INC
Marketing categoryAbbreviated NDA (generic) · App ANDA217605
Dosage form / routeFOR SUSPENSION · ORAL
Active ingredientsFAMOTIDINE (40 mg/5mL)
Marketing started20240315
Package count1

External sources

Source: openFDA. Public-domain (CC0).