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Uline Ibuprofen

NDC 69790-609 · Uline

Generic nameIbuprofen
Dosage formTABLET, 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

69790-609-33 — 50 PACKET in 1 BOX (69790-609-33) / 2 TABLET, COATED in 1 PACKET

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69452-446 — Acetaminophen and Ibuprofen, 69452-447 — Acetaminophen and Ibuprofen, 69452-469 — Acetaminophen and Ibuprofen, 69452-507 — IBUPROFEN AND DIPHENHYDRAMINE HCL, 69452-513 — Ibuprofen, 69517-111 — Ibuprofen, 69607-1970 — Diphenhydramine Citrate, Ibuprofen, 69607-8438 — Ibuprofen, 69618-078 — Ibuprofen, 69729-157 — Ibuprofen, 69790-709 — Ibuprofen, 69822-693 — Ibuprofen 200mg, 69842-092 — Ibuprofen and Pseudoephedrine HCl, 69842-329 — Ibuprofen, 69842-391 — Ibuprofen, 69842-489 — Ibuprofen, 69842-493 — Ibuprofen, 69842-521 — ibuprofen, 69842-643 — Ibuprofen, 69842-649 — Ibuprofen, +1311 more

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