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Ibuprofen

NDC 70512-780 · SOLA Pharmaceuticals, LLC

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

70512-780-10 — 100 TABLET in 1 BOTTLE (70512-780-10)

70512-780-50 — 500 TABLET in 1 BOTTLE (70512-780-50)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70010-068 — Ibuprofen, 70010-131 — Acetaminophen and Ibuprofen, 70010-213 — Acetaminophen and Ibuprofen, 70038-131 — Acetaminophen, 70264-029 — IBUPROFEN, 70264-040 — Acetaminophen 250 mg and Ibuprofen 125 mg, 70264-041 — Ibuprofen, 70264-042 — Ibuprofen, 70264-043 — Ibuprofen, 70264-044 — Ibuprofen, 70512-794 — ibuprofen, 70518-0176 — Ibuprofen, 70518-0761 — Ibuprofen, 70518-1051 — Ibuprofen, 70518-1364 — Ibuprofen, 70518-1409 — Ibuprofen, 70518-2432 — Ibuprofen, 70518-2902 — Ibuprofen, 70518-3178 — Ibuprofen, 70518-3313 — 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.