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Ibuprofen

NDC 68998-011 · Marc Glassman, Inc.

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

68998-011-03 — 1 BOTTLE, PLASTIC in 1 CARTON (68998-011-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68788-8438 — Ibuprofen, 68788-8531 — Ibuprofen, 68788-8590 — Ibuprofen, 68788-8710 — Ibuprofen, 68788-8754 — Ibuprofen, 68788-8757 — Ibuprofen, 68788-8897 — Ibuprofen and famotidine, 68788-9110 — Ibuprofen, 68788-9111 — Ibuprofen, 68788-9112 — Ibuprofen, 68998-012 — Ibuprofen, 68998-109 — Ibuprofen, 68998-110 — Ibuprofen, 68998-185 — Ibuprofen, 68998-320 — Ibuprofen, 69103-2525 — Ibuprofen, 69168-335 — Ibuprofen 200 mg, 69168-368 — Ibuprofen, 69168-381 — Ibuprofen, 69168-382 — Ibuprofen 200mg, +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