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Famotidine

NDC 72657-112 · GLENMARK THERAPEUTICS INC., USA

Generic nameFamotidine
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)FAMOTIDINE
Strength10 mg/1
Pharmacologic classHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
Marketing categoryANDA

Packages

72657-112-20 — 1 BOTTLE in 1 CARTON (72657-112-20) / 200 TABLET, FILM COATED in 1 BOTTLE

72657-112-90 — 1 BOTTLE in 1 CARTON (72657-112-90) / 90 TABLET, FILM COATED in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72288-321 — famotidine, calcium carbonate and magnesium hydroxide, 72288-329 — famotidine, 72288-363 — Famotidine, 72288-774 — famotidine, calcium carbonate and magnesium hydroxide, 72476-150 — famotidine, 72476-299 — famotidine, 72559-032 — Famotidine 20 mg, 72559-038 — Famotidine, 72578-214 — Ibuprofen and Famotidine, 72603-171 — Famotidine, 72657-113 — Famotidine, 72657-132 — Famotidine, 72789-331 — Famotidine, 72789-345 — FAMOTIDINE, 72789-427 — Famotidine, 72789-453 — FAMOTIDINE, 72865-214 — Famotidine, 72865-215 — Famotidine, 73097-017 — Famotidine, Calcium carbonate, and Magnesium hydroxide, 73581-108 — Famotidine 10mg, +401 more

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