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Famotidine

NDC 43386-500 · Lupin Pharmaceuticals,Inc.

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

Packages

43386-500-11 — 50 mL in 1 BOTTLE (43386-500-11)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

41520-617 — Famotidine, Calcium Carbonate, Magnesium Hydroxide, 41520-707 — Famotidine, 41520-901 — Famotidine, 42507-141 — Famotidine, 42507-194 — Famotidine, 42507-321 — famotidine, calcium carbonate and magnesium hydroxide, 42571-433 — FAMOTIDINE, 43063-533 — Famotidine, 43063-695 — Famotidine, 43063-696 — Famotidine, 43598-572 — Famotidine, 43598-824 — Famotidine, 43598-960 — Famotidine, 43602-511 — Famotidine, 43602-544 — Ibuprofen and famotidine, 43602-602 — Famotidine, 46122-345 — famotidine, calcium carbonate and magnesium hydroxide, 46122-735 — Famotidine, 46122-737 — Famotidine, 46708-293 — 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.