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Ibuprofen

NDC 50090-7789 · A-S Medication Solutions

Generic nameIbuprofen
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)IBUPROFEN
Strength400 mg/1
Pharmacologic classAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
Marketing categoryANDA

Packages

50090-7789-0 — 16 TABLET, FILM COATED in 1 BOTTLE (50090-7789-0)

50090-7789-1 — 30 TABLET, FILM COATED in 1 BOTTLE (50090-7789-1)

50090-7789-3 — 100 TABLET, FILM COATED in 1 BOTTLE (50090-7789-3)

50090-7789-4 — 20 TABLET, FILM COATED in 1 BOTTLE (50090-7789-4)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-7274 — Ibuprofen, 50090-7281 — Ibuprofen, 50090-7282 — Ibuprofen, 50090-7283 — Ibuprofen, 50090-7286 — Ibuprofen, 50090-7288 — Ibuprofen, 50090-7320 — Ibuprofen, 50090-7321 — Ibuprofen, 50090-7653 — ibuprofen, 50090-7788 — Ibuprofen, 50090-7905 — Ibuprofen, 50269-000 — IBUPROFEN, 50269-157 — IBUPROFEN, 50332-0130 — Ibuprofen Capsules 200 mg, 50332-0152 — ibuprofen, 50580-100 — Ibuprofen, 50580-120 — Ibuprofen, 50580-184 — Ibuprofen, 50580-198 — Ibuprofen, 50580-208 — Acetaminophen and 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.