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Ibuprofen

NDC 68645-562 · Legacy Pharmaceutical Packaging, LLC

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

68645-562-59 — 60 TABLET, FILM COATED in 1 BOTTLE (68645-562-59)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68210-0800 — IBUPROFEN, 68210-4139 — Ibuprofen, 68210-4140 — Ibuprofen, 68210-4192 — Ibuprofen, 68210-6114 — Ibuprofen, 68210-8100 — Ibuprofen, 68391-212 — Ibuprofen, 68391-604 — Ibuprofen, 68391-610 — Ibuprofen, 68599-8051 — Ibuprofen, 68645-563 — Ibuprofen, 68788-4009 — ACETAMINOPHEN and IBUPROFEN, 68788-4031 — Ibuprofen, 68788-4036 — Ibuprofen, 68788-4039 — Ibuprofen, 68788-4051 — Ibuprofen, 68788-4139 — Ibuprofen, 68788-4140 — Ibuprofen, 68788-8288 — Ibuprofen, 68788-8319 — 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.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels