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Famotidine

NDC 50090-7966 · A-S Medication Solutions

Generic nameFamotidine

Dosage formTABLET

RouteORAL

Active ingredient(s)FAMOTIDINE

Strength40 mg/1

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

Marketing categoryANDA

Packages

50090-7966-0 — 90 TABLET in 1 BOTTLE (50090-7966-0)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-1045 — Famotidine, 50090-1432 — Famotidine, 50090-6582 — FAMOTIDINE, 50090-6790 — Famotidine, 50090-6916 — Famotidine, 50090-6932 — Famotidine, 50090-7178 — Famotidine, 50090-7180 — Famotidine, 50090-7196 — Famotidine, 50090-7829 — FAMOTIDINE, 50090-7981 — FAMOTIDINE, 50090-7982 — FAMOTIDINE, 50268-299 — Famotidine, 50268-304 — Famotidine, 50269-016 — FAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDE, 50269-155 — FAMOTIDINE, 50269-156 — FAMOTIDINE, 50383-913 — Famotidine, 51316-407 — famotidine, calcium carbonate and magnesium hydroxide, 51316-511 — 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