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FAMOTIDINE

NDC 31722-063 · Camber Pharmaceuticals, Inc.

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

31722-063-31 — 50 mL in 1 BOTTLE (31722-063-31)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

25021-754 — Famotidine, 25021-755 — Famotidine, 25021-756 — Famotidine, 27241-249 — Famotidine, 29485-6522 — famotidine, calcium carbonate, and magnesium hydroxide tablet, chewable, 30142-040 — famotidine, calcium carbonate and magnesium hydroxide, 30142-194 — Famotidine, 30142-213 — Famotidine, Calcium Carbonate, Magnesium Hydroxide, 31722-017 — Famotidine, 31722-018 — Famotidine, 31722-315 — Ibuprofen and famotidine, 36800-082 — Famotidine, Calcium Carbonate, Magnesium Hydroxide, 36800-141 — Famotidine, 36800-194 — Famotidine, 36800-616 — famotidine, calcium carbonate and magnesium hydroxide, 37808-042 — Famotidine, 37808-121 — Famotidine, Calcium Carbonate, Magnesium Hydroxide, 37808-301 — Famotidine, 37808-503 — famotidine, calcium carbonate and magnesium hydroxide, 37835-161 — 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.