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Ibuprofen

NDC 60760-929 · St. Mary's Medical Park Pharmacy

Generic nameIbuprofen
Dosage formTABLET
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

60760-929-20 — 20 TABLET in 1 BOTTLE, PLASTIC (60760-929-20)

60760-929-30 — 30 TABLET in 1 BOTTLE, PLASTIC (60760-929-30)

60760-929-60 — 60 TABLET in 1 BOTTLE, PLASTIC (60760-929-60)

60760-929-90 — 90 TABLET in 1 BOTTLE, PLASTIC (60760-929-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

59779-971 — Ibuprofen, 60687-446 — Ibuprofen, 60687-457 — Ibuprofen, 60687-468 — Ibuprofen, 60687-743 — Ibuprofen, 60760-596 — Ibuprofen, 60760-597 — Ibuprofen, 60760-603 — IBUPROFEN, 60760-604 — IBUPROFEN, 60760-844 — Ibuprofen, 61245-084 — Ibuprofen, 61245-085 — Ibuprofen, 61504-109 — Ibuprofen, 61504-110 — Ibuprofen, 61504-185 — Ibuprofen, 61919-463 — IBUOROFEN, 62011-0070 — Ibuprofen and Pseudoephedrine Hydrochloride, 62011-0368 — Ibuprofen, 62011-0399 — Ibuprofen, 62135-400 — 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.