IBUPROFEN

NDC 0615-8310 · NCS HealthCare of KY, LLC dba Vangard Labs

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

0615-8310-39 — 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8310-39)

FDA lists these products with the same active ingredient.

0573-0199 — ibuprofen, phenylephrine hydrochloride, 0573-0207 — ibuprofen, 0573-0232 — ibuprofen, 0573-0290 — ibuprofen, 0573-1174 — ibuprofen, 0573-1711 — ibuprofen, 0573-1769 — ibuprofen, 0573-2160 — ibuprofen and pseudoephedrine hydrochloride, 0573-2161 — chlorpheniramine maleate, ibuprofen, and phenylephrine hydrochloride, 0615-8309 — Ibuprofen, 0615-8311 — Ibuprofen, 0761-0908 — IBUPROFEN, 0904-5309 — Ibuprofen, 0904-5463 — ibuprofen, 0904-5577 — Ibuprofen, 0904-5853 — Ibuprofen, 0904-5854 — Ibuprofen, 0904-5855 — Ibuprofen, 0904-6747 — Ibuprofen, 0904-7587 — 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.