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FAMOTIDINE

NDC 85534-0091 · HAWAII REPACK, INC.

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

85534-0091-0 — 30 TABLET, FILM COATED in 1 BOTTLE (85534-0091-0)

85534-0091-1 — 60 TABLET, FILM COATED in 1 BOTTLE (85534-0091-1)

85534-0091-2 — 90 TABLET, FILM COATED in 1 BOTTLE (85534-0091-2)

85534-0091-3 — 120 TABLET, FILM COATED in 1 BOTTLE (85534-0091-3)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

82804-981 — Famotidine, 82868-077 — Famotidine, 83008-091 — Famotidine, 83059-0005 — Famotidine, 83059-0031 — Famotidine, 83324-003 — famotidine, 83324-008 — famotidine, 83324-116 — Famotidine, 83324-139 — Famotidine, 84126-367 — Famotitine, 85237-1926 — Famotidine, 85237-1948 — Famotidine, Calcium carbonate, and Magnesium hydroxide, 85509-1010 — Ibuprofen and famotidine, 85509-1315 — Ibuprofen and famotidine, 85509-1626 — Ibuprofen and famotidine, 85534-0092 — FAMOTIDINE, 85766-221 — Famotidine, 85766-222 — Famotidine, 85828-443 — Famotidine 20mg, 87441-030 — 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.