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CareOne Acid Relief

NDC 41520-707 · American Sales Company

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

41520-707-71 — 1 BOTTLE in 1 CARTON (41520-707-71) / 50 TABLET, FILM COATED in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

41163-321 — famotidine, calcium carbonate and magnesium hydroxide, 41167-0361 — Famotidine, 41167-0364 — Famotidine, 41226-719 — Famotidine, 41250-284 — famotidine, calcium carbonate and magnesium hydroxide, 41250-493 — famotidine, 41250-690 — Famotidine, Calcium Carbonate, Magnesium Hydroxide, 41250-712 — famotidine, 41520-409 — famotidine, calcium carbonate and magnesium hydroxide, 41520-617 — Famotidine, Calcium Carbonate, Magnesium Hydroxide, 41520-901 — Famotidine, 42507-141 — Famotidine, 42507-194 — Famotidine, 42507-321 — famotidine, calcium carbonate and magnesium hydroxide, 42571-433 — FAMOTIDINE, 43063-533 — Famotidine, 43063-695 — Famotidine, 43063-696 — Famotidine, 43386-500 — Famotidine, 43598-572 — 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.