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Ibuprofen

NDC 69848-011 · Granules USA, Inc.

Generic nameIbuprofen
Dosage formTABLET
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

69848-011-24 — 24 TABLET in 1 BOTTLE (69848-011-24)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69842-493 — Ibuprofen, 69842-521 — ibuprofen, 69842-643 — Ibuprofen, 69842-649 — Ibuprofen, 69842-675 — Acetaminophen, Ibuprofen, 69842-706 — ibuprofen, 69842-745 — Ibuprofen, 69842-870 — IBUPROFEN, DIPHENHYDRAMINE HCL, 69842-892 — Ibuprofen, 69842-913 — Ibuprofen, Diphenhydramine HCl, 69848-012 — Ibuprofen, 69848-588 — Acetaminophen and Ibuprofen, 70000-0003 — Ibuprofen, 70000-0157 — diphenhydramine citrate, ibuprofen, 70000-0175 — Ibuprofen, 70000-0176 — Ibuprofen, 70000-0181 — Ibuprofen, 70000-0239 — Ibuprofen, 70000-0262 — Ibuprofen, 70000-0263 — 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