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Famotidine

NDC 53943-101 · Discount Drug Mart, Inc

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

53943-101-25 — 1 BOTTLE in 1 CARTON (53943-101-25) / 25 TABLET in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51316-816 — Famotidine, 51407-452 — Famotidine, 51407-683 — Famotidine, 51407-684 — Famotidine, 51655-102 — Famotidine, 51655-233 — Famotidine, 51655-312 — Famotidine, 51662-1375 — FAMOTIDINE, 53209-4001 — Famotidine, Calcium carbonate, and Magnesium hydroxide, 53943-100 — Famotidine, 54257-180 — Famotidine, 54257-802 — Famotidine, 54473-411 — Famotidine, 55111-118 — Famotidine, 55111-119 — Famotidine, 55111-120 — Famotidine, 55111-396 — Famotidine, 55154-2628 — Famotidine, 55154-4313 — Famotidine, 55315-435 — 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