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Famotidine

NDC 68001-397 · BluePoint Laboratories

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

68001-397-00 — 100 TABLET, FILM COATED in 1 BOTTLE (68001-397-00)

68001-397-08 — 1000 TABLET, FILM COATED in 1 BOTTLE (68001-397-08)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

67457-433 — Famotidine, 67457-448 — Famotidine, 67457-457 — Famotidine, 67751-202 — Famotidine, Calcium carbonate, and Magnesium hydroxide, 67751-214 — Famotidine, 67877-626 — Ibuprofen and famotidine, 67877-775 — Famotidine, 67877-842 — FAMOTIDINE, 67877-843 — FAMOTIDINE, 67877-889 — FAMOTIDINE, 68001-398 — Famotidine, 68001-494 — Famotidine, 68016-800 — Famotidine, 68016-801 — Famotidine, 68071-2306 — Famotidine, 68071-3201 — Famotidine, 68071-3413 — FAMOTIDINE, 68071-3420 — FAMOTIDINE, 68071-3521 — Famotidine, 68071-3584 — 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.