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Famotidine

NDC 50268-299 · AvPAK

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

50268-299-15 — 50 BLISTER PACK in 1 BOX (50268-299-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-299-11)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-6790 — Famotidine, 50090-6916 — Famotidine, 50090-6932 — Famotidine, 50090-7178 — Famotidine, 50090-7180 — Famotidine, 50090-7196 — Famotidine, 50090-7829 — FAMOTIDINE, 50090-7966 — Famotidine, 50090-7981 — FAMOTIDINE, 50090-7982 — 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, 51316-588 — famotidine, calcium carbonate, magnesium hydroxide, 51316-816 — Famotidine, 51407-452 — 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.