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Ibuprofen

NDC 50090-7286 · 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

50090-7286-0 — 15 TABLET, FILM COATED in 1 BOTTLE (50090-7286-0)

50090-7286-1 — 21 TABLET, FILM COATED in 1 BOTTLE (50090-7286-1)

50090-7286-4 — 28 TABLET, FILM COATED in 1 BOTTLE (50090-7286-4)

50090-7286-5 — 90 TABLET, FILM COATED in 1 BOTTLE (50090-7286-5)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-6645 — Ibuprofen, 50090-6676 — Ibuprofen, 50090-6677 — Ibuprofen, 50090-6886 — Ibuprofen, 50090-7053 — Ibuprofen, 50090-7249 — Ibuprofen, 50090-7274 — Ibuprofen, 50090-7281 — Ibuprofen, 50090-7282 — Ibuprofen, 50090-7283 — Ibuprofen, 50090-7288 — Ibuprofen, 50090-7320 — Ibuprofen, 50090-7321 — Ibuprofen, 50090-7653 — ibuprofen, 50090-7788 — Ibuprofen, 50090-7789 — Ibuprofen, 50090-7905 — Ibuprofen, 50269-000 — IBUPROFEN, 50269-157 — IBUPROFEN, 50332-0130 — Ibuprofen Capsules 200 mg, +1311 more

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