Skip to main content

Famotidine

NDC 83324-139 · Chain Drug Marketing Association INC

Generic nameFamotidine

Dosage formTABLET

RouteORAL

Active ingredient(s)FAMOTIDINE

Strength10 mg/1

Pharmacologic classHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

Marketing categoryANDA

Packages

83324-139-30 — 1 BOTTLE in 1 CARTON (83324-139-30) / 30 TABLET in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

82804-228 — Famotidine, 82804-980 — Famotidine, 82804-981 — Famotidine, 82868-077 — Famotidine, 83008-091 — Famotidine, 83059-0005 — Famotidine, 83059-0031 — Famotidine, 83324-003 — famotidine, 83324-008 — famotidine, 83324-116 — Famotidine, 84126-367 — Famotitine, 85237-1926 — Famotidine, 85237-1948 — Famotidine, Calcium carbonate, and Magnesium hydroxide, 85509-1010 — Ibuprofen and famotidine, 85509-1315 — Ibuprofen and famotidine, 85509-1626 — Ibuprofen and famotidine, 85534-0091 — FAMOTIDINE, 85534-0092 — FAMOTIDINE, 85766-221 — Famotidine, 85766-222 — 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