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Famotidine

NDC 63629-2782 · Bryant Ranch Prepack

Generic nameFamotidine
Dosage formTABLET
RouteORAL
Active ingredient(s)FAMOTIDINE
Strength40 mg/1
Pharmacologic classHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
Marketing categoryANDA

Packages

63629-2782-1 30 TABLET in 1 BOTTLE (63629-2782-1)

63629-2782-2 60 TABLET in 1 BOTTLE (63629-2782-2)

63629-2782-3 100 TABLET in 1 BOTTLE (63629-2782-3)

63629-2782-4 90 TABLET in 1 BOTTLE (63629-2782-4)

63629-2782-5 15 TABLET in 1 BOTTLE (63629-2782-5)

63629-2782-6 120 TABLET in 1 BOTTLE (63629-2782-6)

63629-2782-7 20 TABLET in 1 BOTTLE (63629-2782-7)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

62332-001 — Famotidine, 62332-002 — Famotidine, 63187-129 — Famotidine, 63187-723 — Famotidine, 63187-908 — Famotidine, 63187-999 — Famotidine, 63323-738 — FAMOTIDINE, 63323-739 — Famotidine, 63629-2014 — Famotidine, 63629-2015 — Famotidine, 63629-7013 — Famotidine, 63629-8891 — Ibuprofen and famotidine, 63868-583 — Famotidine, 63868-584 — Famotidine, 63941-009 — Famotidine, 63941-011 — Famotidine, 63981-194 — Famotidine, 64980-623 — Famotidine, 64980-624 — Famotidine, 65862-859 — 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.