FDA NDC Directory · JSON-LD · Markdown

Famotidine

NDC 0641-6023 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerHikma Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA075488
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsFAMOTIDINE (10 mg/mL)
Marketing started20010416
Package count2

External sources

Source: openFDA. Public-domain (CC0).