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FAMOTIDINE

NDC 72865-215 · XLCare Pharmaceuticals, Inc.

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

72865-215-01 — 100 TABLET, FILM COATED in 1 BOTTLE (72865-215-01)

72865-215-05 — 500 TABLET, FILM COATED in 1 BOTTLE (72865-215-05)

72865-215-18 — 180 TABLET, FILM COATED in 1 BOTTLE (72865-215-18)

72865-215-30 — 30 TABLET, FILM COATED in 1 BOTTLE (72865-215-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72578-214 — Ibuprofen and Famotidine, 72603-171 — Famotidine, 72657-112 — Famotidine, 72657-113 — Famotidine, 72657-132 — Famotidine, 72789-331 — Famotidine, 72789-345 — FAMOTIDINE, 72789-427 — Famotidine, 72789-453 — FAMOTIDINE, 72865-214 — Famotidine, 73097-017 — Famotidine, Calcium carbonate, and Magnesium hydroxide, 73581-108 — Famotidine 10mg, 73581-109 — Famotidine 20mg, 76162-300 — famotidine, 76420-712 — FAMOTIDINE, 76420-713 — FAMOTIDINE, 76420-891 — Ibuprofen and famotidine, 79903-115 — famotidine, 80005-119 — FAMOTIDINE, 80425-0329 — 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.