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IBU

NDC 55111-683 · Dr. Reddy's Laboratories Limited

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

55111-683-01 — 100 TABLET in 1 BOTTLE (55111-683-01)

55111-683-05 — 500 TABLET in 1 BOTTLE (55111-683-05)

55111-683-09 — 90 TABLET in 1 BOTTLE (55111-683-09)

55111-683-30 — 30 TABLET in 1 BOTTLE (55111-683-30)

55111-683-50 — 50 TABLET in 1 BOTTLE (55111-683-50)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

53943-292 — Ibuprofen, 53943-637 — Ibuprofen, 53943-682 — Ibuprofen, 54162-941 — Ibuprofen, 54348-825 — IBUPROFEN, 54348-830 — IBUPROFEN, 54348-835 — IBUPROFEN, 54473-306 — Ibuprofen, 55111-565 — Ibuprofen and Diphenhydramine Citrate, 55111-682 — Ibuprofen, 55111-684 — Ibuprofen, 55154-0669 — Ibuprofen, 55154-0741 — Ibuprofen, 55154-1342 — Ibuprofen, 55154-1380 — Ibuprofen, 55154-1577 — Ibuprofen, 55154-2583 — Ibuprofen, 55301-050 — diphenhydramine citrate, ibuprofen, 55301-291 — Ibuprofen, 55301-292 — 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.