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ibuprofen

NDC 50090-5223 · A-S Medication Solutions

Generic nameIbuprofen
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)IBUPROFEN
Strength200 mg/1
Pharmacologic classAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
Marketing categoryANDA

Packages

50090-5223-0 — 50 TABLET, FILM COATED in 1 BOTTLE (50090-5223-0)

50090-5223-3 — 24 TABLET, FILM COATED in 1 BOTTLE (50090-5223-3)

50090-5223-8 — 100 TABLET, FILM COATED in 1 BOTTLE (50090-5223-8)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

49483-716 — Acetaminophen, Ibuprofen, 49884-366 — Ibuprofen and famotidine, 50090-2549 — Ibuprofen, 50090-2597 — Ibuprofen, 50090-2625 — Ibuprofen, 50090-2626 — Ibuprofen, 50090-2629 — Ibuprofen, 50090-3007 — Ibuprofen, 50090-3507 — Ibuprofen Capsules 200 mg, 50090-4129 — Ibuprofen Oral, 50090-5433 — Ibuprofen, 50090-5435 — Ibuprofen, 50090-5444 — Ibuprofen, 50090-5445 — Ibuprofen, 50090-5446 — Ibuprofen, 50090-5818 — Ibuprofen, 50090-5819 — Ibuprofen, 50090-6616 — Ibuprofen, 50090-6645 — Ibuprofen, 50090-6676 — 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.