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Famotidine

NDC 21130-022 · Albertsons Companies

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

21130-022-30 — 1 BOTTLE in 1 CARTON (21130-022-30) / 30 TABLET in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

11822-1014 — famotidine, 11822-1194 — Famotidine, 11822-6123 — famotidine, 11822-6141 — Famotidine, 16837-246 — Famotidine, Calcium Carbonate, and Magnesium Hydroxide, 16837-298 — Famotidine, Calcium carbonate, and Magnesium hydroxide, 16837-855 — Famotidine, 16837-872 — Famotidine, 16837-889 — Famotidine, 16837-891 — famotidine, calcium carbonate, and magnesium hydroxide, 21130-023 — Famotidine, 21130-027 — Famotidine, 21130-033 — Famotidine, 21130-039 — Famotidine, 21130-087 — famotidine, calcium carbonate and magnesium hydroxide, 21130-191 — Famotidine, 21130-249 — Famotidine, 21130-521 — Famotidine, 21130-546 — Famotidine, Calcium Carbonate, Magnesium Hydroxide, 21130-614 — famotidine, calcium carbonate and magnesium hydroxide, +401 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.