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Ibuprofen

NDC 60760-597 · ST. MARY'S MEDICAL PARK PHARMACY

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

60760-597-20 — 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-597-20)

60760-597-28 — 28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-597-28)

60760-597-30 — 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-597-30)

60760-597-40 — 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-597-40)

60760-597-60 — 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-597-60)

60760-597-90 — 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-597-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

59779-647 — Ibuprofen, 59779-660 — Ibuprofen, 59779-685 — Ibuprofen, 59779-897 — Ibuprofen, 59779-971 — Ibuprofen, 60687-446 — Ibuprofen, 60687-457 — Ibuprofen, 60687-468 — Ibuprofen, 60687-743 — Ibuprofen, 60760-596 — Ibuprofen, 60760-603 — IBUPROFEN, 60760-604 — IBUPROFEN, 60760-844 — Ibuprofen, 60760-929 — Ibuprofen, 61245-084 — Ibuprofen, 61245-085 — Ibuprofen, 61504-109 — Ibuprofen, 61504-110 — Ibuprofen, 61504-185 — Ibuprofen, 61919-463 — IBUOROFEN, +1311 more

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