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Famotidine

NDC 51407-683 · Golden State Medical Supply, Inc.

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

51407-683-10 — 36 BOTTLE in 1 BOX (51407-683-10) / 1000 TABLET in 1 BOTTLE

51407-683-18 — 36 BOTTLE in 1 BOX (51407-683-18) / 180 TABLET in 1 BOTTLE

51407-683-25 — 36 BOTTLE in 1 BOX (51407-683-25) / 25 TABLET in 1 BOTTLE

51407-683-30 — 36 BOTTLE in 1 BOX (51407-683-30) / 30 TABLET in 1 BOTTLE

51407-683-50 — 36 BOTTLE in 1 BOX (51407-683-50) / 50 TABLET in 1 BOTTLE

51407-683-90 — 36 BOTTLE in 1 BOX (51407-683-90) / 90 TABLET in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 51316-511 — Famotidine, 51316-588 — famotidine, calcium carbonate, magnesium hydroxide, 51316-816 — Famotidine, 51407-452 — Famotidine, 51407-684 — Famotidine, 51655-102 — Famotidine, 51655-233 — Famotidine, 51655-312 — Famotidine, 51662-1375 — FAMOTIDINE, 53209-4001 — Famotidine, Calcium carbonate, and Magnesium hydroxide, 53943-100 — Famotidine, 53943-101 — Famotidine, 54257-180 — Famotidine, 54257-802 — 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.