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FAMOTIDINE

NDC 60760-843 · ST. MARY'S MEDICAL PARK PHARMACY

Generic nameFAMOTIDINE
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)FAMOTIDINE
Strength40 mg/1
Pharmacologic classHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
Marketing categoryANDA

Packages

60760-843-07 — 7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-843-07)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

59640-023 — famotidine, 59651-701 — FAMOTIDINE, 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, 60760-937 — Famotidine, 61442-121 — 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, +401 more

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