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FAMOTIDINE

NDC 76420-712 · Asclemed USA, Inc.

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

76420-712-01 — 100 TABLET, FILM COATED in 1 BOTTLE (76420-712-01)

76420-712-30 — 30 TABLET, FILM COATED in 1 BOTTLE (76420-712-30)

76420-712-60 — 60 TABLET, FILM COATED in 1 BOTTLE (76420-712-60)

76420-712-90 — 90 TABLET, FILM COATED in 1 BOTTLE (76420-712-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72789-331 — Famotidine, 72789-345 — FAMOTIDINE, 72789-427 — Famotidine, 72789-453 — FAMOTIDINE, 72865-214 — Famotidine, 72865-215 — Famotidine, 73097-017 — Famotidine, Calcium carbonate, and Magnesium hydroxide, 73581-108 — Famotidine 10mg, 73581-109 — Famotidine 20mg, 76162-300 — famotidine, 76420-713 — FAMOTIDINE, 76420-891 — Ibuprofen and famotidine, 79903-115 — famotidine, 80005-119 — FAMOTIDINE, 80425-0329 — Famotidine, 80425-0384 — Ibuprofen and famotidine, 80425-0422 — Ibuprofen and famotidine, 80425-0483 — Ibuprofen and famotidine, 80425-0587 — Ibuprofen and Famotidine, 80425-0589 — 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.