Ibuprofen

NDC 68016-645 · Chain Drug Consortium

FDA lists marketing as ended on 2026-08-31.

Generic nameIbuprofen

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)IBUPROFEN

Strength200 mg/1

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

Marketing categoryANDA

Packages

68016-645-08 — 1 BOTTLE, PLASTIC in 1 CARTON (68016-645-08) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

68016-645-12 — 1 BOTTLE, PLASTIC in 1 CARTON (68016-645-12) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

68016-645-15 — 1 BOTTLE, PLASTIC in 1 CARTON (68016-645-15) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

FDA lists these products with the same active ingredient.

67751-149 — CHLORPHENIRAMINE MALEATE, IBUPROFEN, PHENYLEPHRINE HYDROCHLORIDE, 67751-150 — IBUPROFEN, PHENYLEPHRINE HYDROCHLORIDE, 67751-211 — Ibuprofen, Acetaminophen, 67877-319 — Ibuprofen, 67877-320 — Ibuprofen, 67877-321 — Ibuprofen, 67877-626 — Ibuprofen and famotidine, 68001-521 — Ibuprofen, 68016-057 — IBUPROFEN, DIPHENHYDRAMINE HCL, 68016-634 — Ibuprofen, 68016-813 — Ibuprofen, 68071-1628 — Ibuprofen Oral, 68071-2939 — Ibuprofen, 68071-2947 — Ibuprofen, 68071-2998 — Ibuprofen, 68071-3053 — Ibuprofen, 68071-3415 — Ibuprofen, 68071-3442 — Ibuprofen, 68071-3507 — Ibuprofen, 68071-3552 — 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.