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Ibuprofen

NDC 50090-2626 · A-S Medication Solutions

Generic nameIbuprofen
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)IBUPROFEN
Strength600 mg/1
Pharmacologic classAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
Marketing categoryANDA

Packages

50090-2626-0 — 15 TABLET, FILM COATED in 1 BOTTLE (50090-2626-0)

50090-2626-1 — 21 TABLET, FILM COATED in 1 BOTTLE (50090-2626-1)

50090-2626-4 — 28 TABLET, FILM COATED in 1 BOTTLE (50090-2626-4)

50090-2626-5 — 90 TABLET, FILM COATED in 1 BOTTLE (50090-2626-5)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

49483-604 — Ibuprofen, 49483-610 — IBUPROFEN, 49483-611 — IBUPROFEN, 49483-612 — IBUPROFEN, 49483-700 — Ibuprofen, 49483-716 — Acetaminophen, Ibuprofen, 49884-366 — Ibuprofen and famotidine, 50090-2549 — Ibuprofen, 50090-2597 — Ibuprofen, 50090-2625 — Ibuprofen, 50090-2629 — Ibuprofen, 50090-3007 — Ibuprofen, 50090-3507 — Ibuprofen Capsules 200 mg, 50090-4129 — Ibuprofen Oral, 50090-5223 — Ibuprofen, 50090-5433 — Ibuprofen, 50090-5435 — Ibuprofen, 50090-5444 — Ibuprofen, 50090-5445 — Ibuprofen, 50090-5446 — Ibuprofen, +1311 more

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