Ibuprofen

NDC 68016-634 · Chain Drug Consortium

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

68016-634-00 — 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68016-634-00)

68016-634-05 — 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68016-634-05)

68016-634-10 — 1 BOTTLE, PLASTIC in 1 CARTON (68016-634-10) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

68016-634-24 — 1 BOTTLE, PLASTIC in 1 CARTON (68016-634-24) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

68016-634-25 — 250 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68016-634-25)

68016-634-50 — 1 BOTTLE, PLASTIC in 1 CARTON (68016-634-50) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

FDA lists these products with the same active ingredient.

67751-148 — IBUPROFEN, 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, 68016-645 — 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, +1312 more

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