Ibuprofen

NDC 67877-320 · Ascend Laboratories, LLC

Generic nameIbuprofen

Dosage formTABLET, FILM COATED

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

67877-320-01 — 100 TABLET, FILM COATED in 1 BOTTLE (67877-320-01)

67877-320-05 — 500 TABLET, FILM COATED in 1 BOTTLE (67877-320-05)

67877-320-30 — 30 TABLET, FILM COATED in 1 BOTTLE (67877-320-30)

67877-320-50 — 50 TABLET, FILM COATED in 1 BOTTLE (67877-320-50)

FDA lists these products with the same active ingredient.

67296-2196 — Ibuprofen, 67414-240 — IBUPROFEN, 67751-120 — IBUPROFEN, 67751-146 — IBUPROFEN, 67751-147 — DIPHENHYDRAMINE CITRATE, IBUPROFEN, 67751-148 — IBUPROFEN, 67751-149 — CHLORPHENIRAMINE MALEATE, IBUPROFEN, PHENYLEPHRINE HYDROCHLORIDE, 67751-150 — IBUPROFEN, PHENYLEPHRINE HYDROCHLORIDE, 67751-211 — Ibuprofen, Acetaminophen, 67877-319 — 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, 68071-2947 — 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.