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ibuprofen

NDC 56062-517 · Publix Super Markets Inc

Generic nameIbuprofen
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)IBUPROFEN
Strength200 mg/1
Pharmacologic classAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
Marketing categoryANDA

Packages

56062-517-71 — 1 BOTTLE in 1 CARTON (56062-517-71) / 50 TABLET, FILM COATED in 1 BOTTLE

56062-517-78 — 1 BOTTLE in 1 CARTON (56062-517-78) / 100 TABLET, FILM COATED in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

55910-845 — Ibuprofen, 55910-847 — Ibuprofen, 55910-897 — Ibuprofen, 55910-901 — ibuprofen, 55910-953 — Ibuprofen, 56062-050 — diphenhydramine citrate, ibuprofen, 56062-057 — ibuprofen, 56062-166 — Ibuprofen, 56062-404 — Ibuprofen, 56062-423 — Ibuprofen and Pseudoephedrine Hydrochloride, 56062-530 — Acetaminophen, Ibuprofen, 56062-560 — Ibuprofen capsule, 56062-604 — Ibuprofen, 56062-647 — Ibuprofen, 56062-801 — ibuprofen, 56062-897 — Ibuprofen, 57243-291 — Ibuprofen, 57344-109 — Ibuprofen, 57344-110 — Ibuprofen, 57344-309 — 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.