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FAMOTIDINE

NDC 72205-233 · Novadoz Pharmaceuticals LLC

Generic nameFAMOTIDINE
Dosage formPOWDER, FOR SUSPENSION
RouteORAL
Active ingredient(s)FAMOTIDINE
Strength40 mg/5mL
Pharmacologic classHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
Marketing categoryANDA

Packages

72205-233-84 — 55 mL in 1 BOTTLE (72205-233-84)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72036-026 — Famotidine, 72162-1737 — Famotidine, 72162-2599 — FAMOTIDINE, 72189-141 — FAMOTIDINE, 72189-207 — FAMOTIDINE, 72189-543 — Famotidine, 72189-641 — Ibuprofen Famotidine, 72189-667 — Ibuprofen Famotidine, 72205-145 — Famotidine, 72205-146 — Famotidine, 72288-141 — Famotidine, 72288-151 — famotidine, 72288-194 — Famotidine, 72288-321 — famotidine, calcium carbonate and magnesium hydroxide, 72288-329 — famotidine, 72288-363 — Famotidine, 72288-774 — famotidine, calcium carbonate and magnesium hydroxide, 72476-150 — famotidine, 72476-299 — famotidine, 72559-032 — Famotidine 20 mg, +401 more

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