Famotidine

NDC 61442-121 · Carlsbad Technology, Inc

Generic nameFamotidine

Dosage formTABLET

RouteORAL

Active ingredient(s)FAMOTIDINE

Strength20 mg/1

Pharmacologic classHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

Marketing categoryANDA

Packages

61442-121-01 — 24 BOTTLE in 1 BOX (61442-121-01) / 100 TABLET in 1 BOTTLE

61442-121-05 — 24 BOTTLE in 1 BOX (61442-121-05) / 500 TABLET in 1 BOTTLE

61442-121-10 — 12 BOTTLE in 1 BOX (61442-121-10) / 1000 TABLET in 1 BOTTLE

61442-121-30 — 24 BOTTLE in 1 BOX (61442-121-30) / 30 TABLET in 1 BOTTLE

FDA lists these products with the same active ingredient.

59651-908 — Ibuprofen and famotidine, 59779-141 — Famotidine, 59779-194 — Famotidine, 59779-738 — famotidine, calcium carbonate and magnesium hydroxide, 59779-862 — Famotidine, Calcium Carbonate, Magnesium Hydroxide, 60219-2090 — Famotidine, 60687-595 — Famotidine, 60760-736 — Famotidine, 60760-843 — FAMOTIDINE, 60760-937 — Famotidine, 61442-122 — Famotidine, 62135-807 — famotidine, 62135-808 — famotidine, 62332-001 — Famotidine, 62332-002 — Famotidine, 63187-129 — Famotidine, 63187-723 — Famotidine, 63187-908 — Famotidine, 63187-999 — Famotidine, 63323-738 — FAMOTIDINE, +401 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.