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Ibuprofen

NDC 68071-3793 · NuCare Pharmaceuticals, Inc.

Generic nameIbuprofen
Dosage formTABLET, FILM COATED
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

68071-3793-1 — 21 TABLET, FILM COATED in 1 BOTTLE (68071-3793-1)

68071-3793-3 — 30 TABLET, FILM COATED in 1 BOTTLE (68071-3793-3)

68071-3793-5 — 15 TABLET, FILM COATED in 1 BOTTLE (68071-3793-5)

68071-3793-6 — 60 TABLET, FILM COATED in 1 BOTTLE (68071-3793-6)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 68071-3849 — Ibuprofen, 68071-3937 — Ibuprofen, 68071-3966 — Ibuprofen, 68071-4009 — IBUPROFEN, 68071-4243 — IBUPROFEN, 68071-4459 — IBUPROFEN, 68071-4845 — Ibuprofen, 68071-4887 — Ibuprofen, 68071-4949 — Ibuprofen, 68071-4952 — Ibuprofen, +1311 more

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