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Ibuprofen

NDC 82804-293 · Proficient Rx LP

Generic nameIbuprofen
Dosage formTABLET
RouteORAL
Active ingredient(s)IBUPROFEN
Strength800 mg/1
Pharmacologic classAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
Marketing categoryANDA

Packages

82804-293-20 — 20 TABLET in 1 BOTTLE (82804-293-20)

82804-293-24 — 24 TABLET in 1 BOTTLE (82804-293-24)

82804-293-30 — 30 TABLET in 1 BOTTLE (82804-293-30)

82804-293-40 — 40 TABLET in 1 BOTTLE (82804-293-40)

82804-293-60 — 60 TABLET in 1 BOTTLE (82804-293-60)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

81522-185 — Ibuprofen, 81522-311 — IBUPROFEN, 81522-700 — Ibuprofen, 81522-938 — Ibuprofen, 82179-001 — Ibuprofen, 82179-006 — Ibuprofen, 82501-0604 — Ibuprofen, 82706-032 — Ibuprofen, 82804-137 — Ibuprofen, 82804-227 — 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, 83324-005 — Ibuprofen, 83324-012 — 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.