Skip to main content

Famotidine

NDC 70756-052 · Lifestar Pharma LLC

Generic nameFamotidine
Dosage formTABLET
RouteORAL
Active ingredient(s)FAMOTIDINE
Strength40 mg/1
Pharmacologic classHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
Marketing categoryANDA

Packages

70756-052-11 — 100 TABLET in 1 BOTTLE (70756-052-11)

70756-052-12 — 1000 TABLET in 1 BOTTLE (70756-052-12)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-4394 — Famotidine, 70518-4395 — Famotidine, 70518-4574 — FAMOTIDINE, 70518-4580 — Ibuprofen and famotidine, 70677-1100 — famotidine, calcium carbonate and magnesium hydroxide, 70677-1101 — Famotidine, 70677-1102 — Famotidine, 70710-1683 — Famotidine, 70710-1684 — Famotidine, 70756-051 — Famotidine, 70771-1702 — Famotidine, 70771-1703 — Famotidine, 70771-1924 — Ibuprofen and Famotidine, 70954-316 — Famotidine, 71205-257 — Famotidine, 71205-276 — Famotidine, 71205-535 — Famotidine, 71205-634 — Famotidine, 71205-637 — Famotidine, 71205-663 — 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.