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Ibuprofen

NDC 82804-137 · Proficient Rx LP

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

82804-137-15 — 15 TABLET, FILM COATED in 1 BOTTLE (82804-137-15)

82804-137-30 — 30 TABLET, FILM COATED in 1 BOTTLE (82804-137-30)

82804-137-60 — 60 TABLET, FILM COATED in 1 BOTTLE (82804-137-60)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

81033-019 — Ibuprofen, 81522-119 — Ibuprofen, 81522-185 — Ibuprofen, 81522-311 — IBUPROFEN, 81522-700 — Ibuprofen, 81522-938 — Ibuprofen, 82179-001 — Ibuprofen, 82179-006 — Ibuprofen, 82501-0604 — Ibuprofen, 82706-032 — Ibuprofen, 82804-227 — Ibuprofen, 82804-293 — Ibuprofen, 82868-069 — Ibuprofen, 83008-050 — Ibuprofen, 83008-066 — Ibuprofen, 83059-0020 — Ibuprofen, 83059-0049 — Ibuprofen, 83059-0082 — Ibuprofen, 83059-0165 — Ibuprofen, 83209-464 — 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.