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Famotidine

NDC 50090-6790 · A-S Medication Solutions

Generic nameFamotidine
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)FAMOTIDINE
Strength40 mg/1
Pharmacologic classHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
Marketing categoryANDA

Packages

50090-6790-0 — 30 TABLET, FILM COATED in 1 BOTTLE (50090-6790-0)

50090-6790-1 — 90 TABLET, FILM COATED in 1 BOTTLE (50090-6790-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

49035-507 — Famotidine, 49035-546 — Famotidine, Calcium Carbonate, Magnesium Hydroxide, 49035-589 — Famotidine, 49035-650 — Famotidine, 49483-720 — Famotidine, 49884-366 — Ibuprofen and famotidine, 50090-1044 — Famotidine, 50090-1045 — Famotidine, 50090-1432 — Famotidine, 50090-6582 — FAMOTIDINE, 50090-6916 — Famotidine, 50090-6932 — Famotidine, 50090-7178 — Famotidine, 50090-7180 — Famotidine, 50090-7196 — Famotidine, 50090-7829 — FAMOTIDINE, 50090-7966 — Famotidine, 50090-7981 — FAMOTIDINE, 50090-7982 — FAMOTIDINE, 50268-299 — 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.