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Famotidine

NDC 65862-860 · Aurobindo Pharma Limited

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

65862-860-01 — 100 TABLET, FILM COATED in 1 BOTTLE (65862-860-01)

65862-860-05 — 500 TABLET, FILM COATED in 1 BOTTLE (65862-860-05)

65862-860-30 — 30 TABLET, FILM COATED in 1 BOTTLE (65862-860-30)

65862-860-78 — 10 BLISTER PACK in 1 CARTON (65862-860-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-860-10)

65862-860-99 — 1000 TABLET, FILM COATED in 1 BOTTLE (65862-860-99)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63629-7013 — Famotidine, 63629-8891 — Ibuprofen and famotidine, 63868-583 — Famotidine, 63868-584 — Famotidine, 63941-009 — Famotidine, 63941-011 — Famotidine, 63981-194 — Famotidine, 64980-623 — Famotidine, 64980-624 — Famotidine, 65862-859 — 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, 67296-2186 — Famotidine, 67296-2264 — 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.