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Famotidine

NDC 57896-319 · Geri-Care Pharmaceutical Corp

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

57896-319-01 — 1 BOTTLE in 1 CARTON (57896-319-01) / 100 TABLET, FILM COATED in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

55910-141 — Famotidine, 55910-194 — Famotidine, 55910-665 — famotidine, 55910-808 — famotidine, calcium carbonate and magnesium hydroxide, 55910-814 — famotidine, 56062-088 — Famotidine, 56062-141 — Famotidine, 56062-194 — Famotidine, 56062-263 — famotidine, calcium carbonate and magnesium hydroxide, 57896-317 — Famotidine, 58602-705 — Famotidine, 58602-706 — Famotidine, 58602-828 — Famotidine, 58602-829 — Famotidine, 58602-859 — Famotidine, 59640-001 — famotidine, 59640-023 — famotidine, 59651-701 — FAMOTIDINE, 59651-908 — Ibuprofen and famotidine, 59779-141 — 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.