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acid relief

NDC 11822-1014 · Rite Aid Corporation

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

11822-1014-0 — 1 BOTTLE in 1 CARTON (11822-1014-0) / 50 TABLET, FILM COATED in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0641-6022 — Famotidine, 0641-6023 — Famotidine, 0832-6045 — Famotidine, 0904-5529 — Famotidine, 0904-5780 — Famotidine, 0904-7193 — Famotidine, 10267-5689 — Famotidine, 10267-5690 — Famotidine, 11673-697 — Famotidine, 11822-0500 — famotidine, calcium carbonate and magnesium hydroxide, 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, 21130-022 — 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.