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Famotidine

NDC 71335-2805 · Bryant Ranch Prepack

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

71335-2805-0 40 TABLET, FILM COATED in 1 BOTTLE (71335-2805-0)

71335-2805-1 30 TABLET, FILM COATED in 1 BOTTLE (71335-2805-1)

71335-2805-2 60 TABLET, FILM COATED in 1 BOTTLE (71335-2805-2)

71335-2805-3 20 TABLET, FILM COATED in 1 BOTTLE (71335-2805-3)

71335-2805-4 90 TABLET, FILM COATED in 1 BOTTLE (71335-2805-4)

71335-2805-5 100 TABLET, FILM COATED in 1 BOTTLE (71335-2805-5)

71335-2805-6 10 TABLET, FILM COATED in 1 BOTTLE (71335-2805-6)

71335-2805-7 120 TABLET, FILM COATED in 1 BOTTLE (71335-2805-7)

71335-2805-8 50 TABLET, FILM COATED in 1 BOTTLE (71335-2805-8)

71335-2805-9 14 TABLET, FILM COATED in 1 BOTTLE (71335-2805-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71205-663 — Famotidine, 71205-781 — Famotidine, 71335-0231 — Famotidine, 71335-0370 — Famotidine, 71335-0409 — Famotidine, 71335-1520 — Famotidine, 71335-1950 — Famotidine, 71335-2190 — Famotidine, 71335-2442 — FAMOTIDINE, 71335-2527 — Famotidine, 71335-9615 — Famotidine, 71335-9724 — FAMOTIDINE, 71335-9748 — FAMOTIDINE, 71610-399 — Famotidine, 71610-470 — Famotidine, 71821-010 — Famotidine, 71821-012 — Famotidine, 71872-7220 — Famotidine, 71872-7235 — Famotidine, 71872-7366 — 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.