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Famotidine

NDC 72189-543 · Direct_Rx

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

72189-543-20 — 20 TABLET, FILM COATED in 1 BOTTLE (72189-543-20)

72189-543-30 — 30 TABLET, FILM COATED in 1 BOTTLE (72189-543-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71821-010 — Famotidine, 71821-012 — Famotidine, 71872-7220 — Famotidine, 71872-7235 — Famotidine, 71872-7366 — Famotidine, 72036-026 — Famotidine, 72162-1737 — Famotidine, 72162-2599 — FAMOTIDINE, 72189-141 — FAMOTIDINE, 72189-207 — 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, 72288-321 — famotidine, calcium carbonate and magnesium hydroxide, 72288-329 — 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.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels