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Famotidine

NDC 67296-2186 · Redpharm Drug

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

67296-2186-3 — 30 TABLET, FILM COATED in 1 BOTTLE (67296-2186-3)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 66715-9758 — Famotidine tablet, film-coated, 66715-9822 — Famotidine, Calcium Carbonate, Magnesium Hydroxide Chewable Tablet, 67296-2133 — Famotidine, 67296-2264 — Famotidine, 67457-433 — Famotidine, 67457-448 — Famotidine, 67457-457 — Famotidine, 67751-202 — Famotidine, Calcium carbonate, and Magnesium hydroxide, 67751-214 — Famotidine, 67877-626 — Ibuprofen and famotidine, 67877-775 — Famotidine, 67877-842 — FAMOTIDINE, 67877-843 — 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.