FDA NDC Directory · JSON-LD · Markdown

Famotidine

NDC 50383-913 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SOLUTION

Labeler / ManufacturerAkorn
Marketing categoryAbbreviated NDA (generic) · App ANDA201995
Dosage form / routePOWDER, FOR SOLUTION · ORAL
Active ingredientsFAMOTIDINE (40 mg/5mL)
Marketing started20160316
Package count1

External sources

Source: openFDA. Public-domain (CC0).