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acid controller

NDC 21130-521 · Safeway

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

21130-521-82 — 1 BOTTLE in 1 CARTON (21130-521-82) / 200 TABLET, FILM COATED in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

16837-889 — Famotidine, 16837-891 — famotidine, calcium carbonate, and magnesium hydroxide, 21130-022 — Famotidine, 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, 21130-546 — Famotidine, Calcium Carbonate, Magnesium Hydroxide, 21130-614 — famotidine, calcium carbonate and magnesium hydroxide, 21130-771 — Famotidine, 21130-777 — Famotidine, 21130-786 — Famotidine, Calcium Carbonate, Magnesium Hydroxide, 25000-086 — Famotidine 10 mg, 25000-087 — Famotidine 20 mg, 25000-124 — Famotidine 20 mg, 25021-753 — Famotidine, 25021-754 — 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.