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Famotidine

NDC 46122-735 · Amerisource Bergen

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

46122-735-65 — 1 BOTTLE in 1 CARTON (46122-735-65) / 30 TABLET, FILM COATED in 1 BOTTLE

46122-735-75 — 1 BOTTLE in 1 CARTON (46122-735-75) / 90 TABLET, FILM COATED in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

43063-695 — Famotidine, 43063-696 — Famotidine, 43386-500 — Famotidine, 43598-572 — Famotidine, 43598-824 — Famotidine, 43598-960 — Famotidine, 43602-511 — Famotidine, 43602-544 — Ibuprofen and famotidine, 43602-602 — Famotidine, 46122-345 — famotidine, calcium carbonate and magnesium hydroxide, 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, 49035-589 — Famotidine, 49035-650 — 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.