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Ibuprofen

NDC 71610-968 · Aphena Pharma Solutions - Tennessee, LLC

Generic nameIbuprofen
Dosage formTABLET
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

71610-968-53 — 60 TABLET in 1 BOTTLE (71610-968-53)

71610-968-60 — 90 TABLET in 1 BOTTLE (71610-968-60)

71610-968-80 — 180 TABLET in 1 BOTTLE (71610-968-80)

71610-968-92 — 270 TABLET in 1 BOTTLE (71610-968-92)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71610-890 — Ibuprofen, 71610-891 — Ibuprofen, 71610-892 — Ibuprofen, 71610-895 — Ibuprofen, 71610-897 — Ibuprofen, 71610-898 — Ibuprofen, 71610-901 — Ibuprofen, 71610-902 — Ibuprofen, 71610-916 — Ibuprofen, 71610-967 — Ibuprofen, 71610-969 — Ibuprofen, 71679-111 — Ibuprofen, 71921-180 — Ibuprofen, 71921-181 — Ibuprofen, 71921-182 — Ibuprofen, 72036-015 — Ibuprofen, 72036-109 — Ibuprofen, 72036-110 — Ibuprofen, 72036-185 — Ibuprofen, 72036-211 — 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.