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ACID REDUCER

NDC 51316-511 · CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED

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

51316-511-63 — 1 BOTTLE in 1 CARTON (51316-511-63) / 25 TABLET, FILM COATED in 1 BOTTLE

51316-511-71 — 1 BOTTLE in 1 CARTON (51316-511-71) / 50 TABLET, FILM COATED in 1 BOTTLE

51316-511-78 — 1 BOTTLE in 1 CARTON (51316-511-78) / 100 TABLET, FILM COATED in 1 BOTTLE

51316-511-98 — 1 BOTTLE in 1 CARTON (51316-511-98) / 75 TABLET, FILM COATED in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-7966 — Famotidine, 50090-7981 — FAMOTIDINE, 50090-7982 — FAMOTIDINE, 50268-299 — Famotidine, 50268-304 — Famotidine, 50269-016 — FAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDE, 50269-155 — FAMOTIDINE, 50269-156 — FAMOTIDINE, 50383-913 — Famotidine, 51316-407 — famotidine, calcium carbonate and magnesium hydroxide, 51316-588 — famotidine, calcium carbonate, magnesium hydroxide, 51316-816 — Famotidine, 51407-452 — Famotidine, 51407-683 — Famotidine, 51407-684 — Famotidine, 51655-102 — Famotidine, 51655-233 — Famotidine, 51655-312 — Famotidine, 51662-1375 — FAMOTIDINE, 53209-4001 — 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.