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Famotidine

NDC 25021-756 · Sagent Pharmaceuticals

Generic nameFamotidine
Dosage formINJECTION, SOLUTION
RouteINTRAVENOUS
Active ingredient(s)FAMOTIDINE
Strength4 mg/mL
Pharmacologic classHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
Marketing categoryNDA

Packages

25021-756-10 — 10 VIAL in 1 CARTON (25021-756-10) / 10 mL in 1 VIAL

25021-756-50 — 1 VIAL in 1 CARTON (25021-756-50) / 50 mL in 1 VIAL

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

21130-614 — famotidine, calcium carbonate and magnesium hydroxide, 21130-771 — Famotidine, 21130-777 — Famotidine, 21130-786 — Famotidine, Calcium Carbonate, Magnesium Hydroxide, 25000-086 — Famotidine 10 mg, 25000-087 — Famotidine 20 mg, 25000-124 — Famotidine 20 mg, 25021-753 — Famotidine, 25021-754 — Famotidine, 25021-755 — 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, 31722-063 — FAMOTIDINE, 31722-315 — Ibuprofen and famotidine, 36800-082 — Famotidine, Calcium Carbonate, Magnesium Hydroxide, +401 more

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