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Famotidine

NDC 68788-8889 · Preferred Pharmaceuticals Inc.

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

68788-8889-1 — 100 TABLET, FILM COATED in 1 BOTTLE (68788-8889-1)

68788-8889-3 — 30 TABLET, FILM COATED in 1 BOTTLE (68788-8889-3)

68788-8889-6 — 60 TABLET, FILM COATED in 1 BOTTLE (68788-8889-6)

68788-8889-9 — 90 TABLET, FILM COATED in 1 BOTTLE (68788-8889-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68391-300 — Famotidine, 68475-400 — famotidine, 68645-594 — Famotidine, 68788-4021 — Famotidine, 68788-4088 — Famotidine, 68788-4119 — Famotidine, 68788-4144 — Famotidine, 68788-8485 — FAMOTIDINE, 68788-8518 — FAMOTIDINE, 68788-8733 — Famotidine, 68788-8897 — Ibuprofen and famotidine, 69168-443 — Famotidine, 69168-445 — Famotidine, 69230-326 — famotidine, 69230-327 — famotidine, 69238-2090 — Famotidine, 69256-002 — Famotidine, 69306-266 — Ibuprofen and famotidine, 69367-400 — Famotidine, 69367-401 — 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.