Ibuprofen

NDC 68071-2947 · NuCare Pharmaceuticals,Inc.

Generic nameIbuprofen

Dosage formTABLET

RouteORAL

Active ingredient(s)IBUPROFEN

Strength600 mg/1

Pharmacologic classAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]

Marketing categoryANDA

Packages

68071-2947-1 21 TABLET in 1 BOTTLE (68071-2947-1)

68071-2947-2 20 TABLET in 1 BOTTLE (68071-2947-2)

68071-2947-3 30 TABLET in 1 BOTTLE (68071-2947-3)

68071-2947-4 40 TABLET in 1 BOTTLE (68071-2947-4)

68071-2947-5 50 TABLET in 1 BOTTLE (68071-2947-5)

68071-2947-6 60 TABLET in 1 BOTTLE (68071-2947-6)

68071-2947-9 90 TABLET in 1 BOTTLE (68071-2947-9)

FDA lists these products with the same active ingredient.

67877-320 — Ibuprofen, 67877-321 — Ibuprofen, 67877-626 — Ibuprofen and famotidine, 68001-521 — Ibuprofen, 68016-057 — IBUPROFEN, DIPHENHYDRAMINE HCL, 68016-634 — Ibuprofen, 68016-645 — Ibuprofen, 68016-813 — Ibuprofen, 68071-1628 — Ibuprofen Oral, 68071-2939 — Ibuprofen, 68071-2998 — Ibuprofen, 68071-3053 — Ibuprofen, 68071-3415 — Ibuprofen, 68071-3442 — Ibuprofen, 68071-3507 — Ibuprofen, 68071-3552 — Ibuprofen, 68071-3589 — Ibuprofen, 68071-3679 — Ibuprofen, 68071-3696 — Ibuprofen, 68071-3778 — Ibuprofen, +1312 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.