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Famotidine

NDC 63629-7013 · Bryant Ranch Prepack

Generic nameFamotidine
Dosage formTABLET
RouteORAL
Active ingredient(s)FAMOTIDINE
Strength20 mg/1
Pharmacologic classHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
Marketing categoryANDA

Packages

63629-7013-1 — 30 TABLET in 1 BOTTLE (63629-7013-1)

63629-7013-2 — 60 TABLET in 1 BOTTLE (63629-7013-2)

63629-7013-3 — 90 TABLET in 1 BOTTLE (63629-7013-3)

63629-7013-4 — 10 TABLET in 1 BOTTLE (63629-7013-4)

63629-7013-5 — 20 TABLET in 1 BOTTLE (63629-7013-5)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 63629-2782 — 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, 65862-860 — Famotidine, +401 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.