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Famotidine

NDC 58602-829 · Aurohealth LLC

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

58602-829-21 — 1 BOTTLE in 1 CARTON (58602-829-21) / 100 TABLET, FILM COATED in 1 BOTTLE

58602-829-34 — 1 BOTTLE in 1 CARTON (58602-829-34) / 200 TABLET, FILM COATED in 1 BOTTLE

58602-829-50 — 1 BOTTLE in 1 CARTON (58602-829-50) / 85 TABLET, FILM COATED in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

55910-814 — famotidine, 56062-088 — Famotidine, 56062-141 — Famotidine, 56062-194 — Famotidine, 56062-263 — famotidine, calcium carbonate and magnesium hydroxide, 57896-317 — Famotidine, 57896-319 — Famotidine, 58602-705 — Famotidine, 58602-706 — Famotidine, 58602-828 — Famotidine, 58602-859 — Famotidine, 59640-001 — famotidine, 59640-023 — famotidine, 59651-701 — FAMOTIDINE, 59651-908 — Ibuprofen and famotidine, 59779-141 — Famotidine, 59779-194 — Famotidine, 59779-738 — famotidine, calcium carbonate and magnesium hydroxide, 59779-862 — Famotidine, Calcium Carbonate, Magnesium Hydroxide, 60219-2090 — 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.