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Famotidine

NDC 31722-017 · Camber Pharmaceuticals, 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

31722-017-01 — 100 TABLET, FILM COATED in 1 BOTTLE (31722-017-01)

31722-017-10 — 1000 TABLET, FILM COATED in 1 BOTTLE (31722-017-10)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

25000-124 — Famotidine 20 mg, 25021-753 — Famotidine, 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, 31722-018 — Famotidine, 31722-063 — 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, +401 more

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