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FAMOTIDINE

NDC 72189-141 · direct rx

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

72189-141-60 — 60 TABLET in 1 BOTTLE (72189-141-60)

72189-141-90 — 90 TABLET in 1 BOTTLE (72189-141-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71610-399 — Famotidine, 71610-470 — Famotidine, 71821-010 — Famotidine, 71821-012 — Famotidine, 71872-7220 — Famotidine, 71872-7235 — Famotidine, 71872-7366 — Famotidine, 72036-026 — Famotidine, 72162-1737 — Famotidine, 72162-2599 — FAMOTIDINE, 72189-207 — FAMOTIDINE, 72189-543 — Famotidine, 72189-641 — Ibuprofen Famotidine, 72189-667 — Ibuprofen Famotidine, 72205-145 — Famotidine, 72205-146 — Famotidine, 72205-233 — FAMOTIDINE, 72288-141 — Famotidine, 72288-151 — famotidine, 72288-194 — 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.