Ibuprofen and famotidine

NDC 76420-891 · Asclemed USA, Inc.

Generic nameIbuprofen and famotidine

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)IBUPROFEN, FAMOTIDINE

Strength26.6; 800 mg/1; mg/1

Pharmacologic classAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC], Nonsteroidal Anti-inflammatory Drug [EPC]

Marketing categoryANDA

Packages

76420-891-01 — 100 TABLET, FILM COATED in 1 BOTTLE (76420-891-01)

76420-891-05 — 500 TABLET, FILM COATED in 1 BOTTLE (76420-891-05)

76420-891-06 — 6 BLISTER PACK in 1 CARTON (76420-891-06) / 1 TABLET, FILM COATED in 1 BLISTER PACK

76420-891-30 — 30 TABLET, FILM COATED in 1 BOTTLE (76420-891-30)

76420-891-60 — 60 TABLET, FILM COATED in 1 BOTTLE (76420-891-60)

76420-891-90 — 90 TABLET, FILM COATED in 1 BOTTLE (76420-891-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

76282-714 — Ibuprofen, 76420-415 — ibuprofen, 76420-575 — Ibuprofen, 76420-576 — Ibuprofen, 76420-577 — Ibuprofen, 76420-712 — FAMOTIDINE, 76420-713 — FAMOTIDINE, 76420-846 — Ibuprofen, 76420-847 — Ibuprofen, 76420-848 — Ibuprofen, 79395-003 — Ibuprofen, 79481-0152 — acetaminophen, ibuprofen, 79481-0392 — Ibuprofen, 79481-0419 — ibuprofen, 79481-0423 — Ibuprofen, 79481-0503 — Acetaminophen, Ibuprofen, 79481-3000 — Ibuprofen, 79481-6501 — Acetaminophen and Ibuprofen, 79903-115 — famotidine, 79903-148 — Acetaminophen, Ibuprofen, +1712 more

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