famotidine

NDC 62135-807 · Chartwell RX, LLC

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

62135-807-90 — 90 TABLET, FILM COATED in 1 BOTTLE (62135-807-90)

FDA lists these products with the same active ingredient.

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, 61442-121 — Famotidine, 61442-122 — 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, 63323-739 — Famotidine, 63629-2014 — 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.