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Famotidine

NDC 63941-011 · Best Choice

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

63941-011-53 — 1 BOTTLE in 1 CARTON (63941-011-53) / 25 TABLET, FILM COATED in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63323-738 — FAMOTIDINE, 63323-739 — Famotidine, 63629-2014 — Famotidine, 63629-2015 — Famotidine, 63629-2782 — Famotidine, 63629-7013 — Famotidine, 63629-8891 — Ibuprofen and famotidine, 63868-583 — Famotidine, 63868-584 — Famotidine, 63941-009 — Famotidine, 63981-194 — Famotidine, 64980-623 — Famotidine, 64980-624 — Famotidine, 65862-859 — Famotidine, 65862-860 — Famotidine, 66715-6422 — Famotidine, Calcium Carbonate, Magnesium Hydroxide Chewable Tablet, 66715-6458 — Famotidine tablet, film-coated, 66715-6522 — Famotidine, Calcium Carbonate, Magnesium Hydroxide Chewable Tablet, 66715-7822 — Famotidine, Calcium Carbonate, Magnesium Hydroxide Chewable Tablet, 66715-9748 — 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.