Skip to main content

Famotidine

NDC 70000-0049 · LEADER/ CARDINAL HEALTH 110, INC.

Generic nameFamotidine
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)FAMOTIDINE
Strength20 mg/1
Pharmacologic classHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
Marketing categoryANDA

Packages

70000-0049-1 — 1 BOTTLE in 1 CARTON (70000-0049-1) / 25 TABLET, FILM COATED in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69256-002 — Famotidine, 69306-266 — Ibuprofen and famotidine, 69367-400 — Famotidine, 69367-401 — Famotidine, 69842-063 — Famotidine, 69842-087 — Famotidine, 69842-659 — famotidine, 69842-924 — Famotidine, 69842-928 — Famotidine, 70000-0048 — Famotidine, 70000-0416 — Famotidine, Calcium Carbonate, Magnesium Hydroxide, 70000-0582 — famotidine, calcium carbonate and magnesium hydroxide, 70000-0654 — Famotidine, 70000-0710 — Famotidine, 70264-034 — famotidine, calcium carbonate, and magnesium hydroxide, 70377-113 — FAMOTIDINE, 70518-3829 — FAMOTIDINE, 70518-4084 — FAMOTIDINE, 70518-4394 — Famotidine, 70518-4395 — Famotidine, +401 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.