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Famotidine

NDC 55111-119 · Dr.Reddy's Laboratories Limited

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

55111-119-01 — 100 TABLET, FILM COATED in 1 BOTTLE (55111-119-01)

55111-119-10 — 1000 TABLET, FILM COATED in 1 BOTTLE (55111-119-10)

55111-119-30 — 30 TABLET, FILM COATED in 1 BOTTLE (55111-119-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51655-233 — Famotidine, 51655-312 — Famotidine, 51662-1375 — FAMOTIDINE, 53209-4001 — Famotidine, Calcium carbonate, and Magnesium hydroxide, 53943-100 — Famotidine, 53943-101 — Famotidine, 54257-180 — Famotidine, 54257-802 — Famotidine, 54473-411 — Famotidine, 55111-118 — Famotidine, 55111-120 — Famotidine, 55111-396 — Famotidine, 55154-2628 — Famotidine, 55154-4313 — Famotidine, 55315-435 — Famotidine, 55319-057 — Famotidine, 55319-408 — Famotidine, 55319-409 — Famotidine, 55319-426 — Famotidine, 55319-427 — 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.