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Maximum Strength Acid Reducer

NDC 11673-697 · TARGET CORPORATION

Generic nameFamotidine
Dosage formTABLET
RouteORAL
Active ingredient(s)FAMOTIDINE
Strength20 mg/1
Pharmacologic classHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
Marketing categoryANDA

Packages

11673-697-01 — 2 BOTTLE in 1 CARTON (11673-697-01) / 50 TABLET in 1 BOTTLE

11673-697-05 — 1 BOTTLE in 1 CARTON (11673-697-05) / 50 TABLET in 1 BOTTLE

11673-697-20 — 1 BOTTLE in 1 CARTON (11673-697-20) / 200 TABLET in 1 BOTTLE

11673-697-52 — 5 BLISTER PACK in 1 CARTON (11673-697-52) / 5 TABLET in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0615-8559 — Famotidine, 0641-6021 — Famotidine, 0641-6022 — Famotidine, 0641-6023 — Famotidine, 0832-6045 — Famotidine, 0904-5529 — Famotidine, 0904-5780 — Famotidine, 0904-7193 — Famotidine, 10267-5689 — Famotidine, 10267-5690 — Famotidine, 11822-0500 — famotidine, calcium carbonate and magnesium hydroxide, 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, +401 more

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