Ibuprofen and Famotidine

NDC 80425-0587 · Advanced Rx of Tennessee, LLC

Generic nameIbuprofen and Famotidine

Dosage formTABLET

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

80425-0587-1 — 30 TABLET in 1 BOTTLE (80425-0587-1)

80425-0587-2 — 60 TABLET in 1 BOTTLE (80425-0587-2)

80425-0587-3 — 90 TABLET in 1 BOTTLE (80425-0587-3)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

80425-0243 — Ibuprofen, 80425-0329 — Famotidine, 80425-0384 — Ibuprofen and famotidine, 80425-0393 — Ibuprofen, 80425-0422 — Ibuprofen and famotidine, 80425-0424 — Ibuprofen, 80425-0426 — Ibuprofen, 80425-0483 — Ibuprofen and famotidine, 80425-0537 — ibuprofen, 80425-0553 — Ibuprofen, 80425-0589 — Famotidine, 81033-019 — Ibuprofen, 81522-119 — Ibuprofen, 81522-185 — Ibuprofen, 81522-311 — IBUPROFEN, 81522-700 — Ibuprofen, 81522-938 — Ibuprofen, 82179-001 — Ibuprofen, 82179-006 — Ibuprofen, 82442-321 — famotidine, calcium carbonate and magnesium hydroxide, +1712 more

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