Skip to main content

Famotidine

NDC 49035-589 · Wal-Mart Stores, Inc.

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

49035-589-19 — 1 BOTTLE in 1 CARTON (49035-589-19) / 90 TABLET, FILM COATED in 1 BOTTLE

49035-589-77 — 1 BOTTLE in 1 CARTON (49035-589-77) / 30 TABLET, FILM COATED in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

46122-345 — famotidine, calcium carbonate and magnesium hydroxide, 46122-735 — Famotidine, 46122-737 — Famotidine, 46708-293 — Famotidine, 46708-294 — Famotidine, 48433-150 — Famotidine, 49035-321 — famotidine, calcium carbonate and magnesium hydroxide, 49035-505 — Famotidine, 49035-507 — Famotidine, 49035-546 — Famotidine, Calcium Carbonate, Magnesium Hydroxide, 49035-650 — Famotidine, 49483-720 — Famotidine, 49884-366 — Ibuprofen and famotidine, 50090-1044 — Famotidine, 50090-1045 — Famotidine, 50090-1432 — Famotidine, 50090-6582 — FAMOTIDINE, 50090-6790 — Famotidine, 50090-6916 — Famotidine, 50090-6932 — 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.