Ibuprofen

NDC 68071-3415 · NuCare Pharmaceuticals,Inc.

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

68071-3415-6 — 6 TABLET in 1 BOTTLE (68071-3415-6)

FDA lists these products with the same active ingredient.

68001-521 — Ibuprofen, 68016-057 — IBUPROFEN, DIPHENHYDRAMINE HCL, 68016-634 — Ibuprofen, 68016-645 — Ibuprofen, 68016-813 — Ibuprofen, 68071-1628 — Ibuprofen Oral, 68071-2939 — Ibuprofen, 68071-2947 — Ibuprofen, 68071-2998 — Ibuprofen, 68071-3053 — Ibuprofen, 68071-3442 — Ibuprofen, 68071-3507 — Ibuprofen, 68071-3552 — Ibuprofen, 68071-3589 — Ibuprofen, 68071-3679 — Ibuprofen, 68071-3696 — Ibuprofen, 68071-3778 — Ibuprofen, 68071-3793 — Ibuprofen, 68071-3849 — Ibuprofen, 68071-3937 — Ibuprofen, +1312 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.