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Famotidine

NDC 63187-723 · Proficient Rx LP

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

63187-723-00 — 100 TABLET in 1 BOTTLE (63187-723-00)

63187-723-06 — 6 TABLET in 1 BOTTLE (63187-723-06)

63187-723-10 — 10 TABLET in 1 BOTTLE (63187-723-10)

63187-723-30 — 30 TABLET in 1 BOTTLE (63187-723-30)

63187-723-60 — 60 TABLET in 1 BOTTLE (63187-723-60)

63187-723-90 — 90 TABLET in 1 BOTTLE (63187-723-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

60760-736 — Famotidine, 60760-843 — FAMOTIDINE, 60760-937 — Famotidine, 61442-121 — Famotidine, 61442-122 — Famotidine, 62135-807 — famotidine, 62135-808 — famotidine, 62332-001 — Famotidine, 62332-002 — Famotidine, 63187-129 — Famotidine, 63187-908 — Famotidine, 63187-999 — Famotidine, 63323-738 — FAMOTIDINE, 63323-739 — Famotidine, 63629-2014 — Famotidine, 63629-2015 — Famotidine, 63629-2782 — Famotidine, 63629-7013 — Famotidine, 63629-8891 — Ibuprofen and famotidine, 63868-583 — 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.