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Ibuprofen

NDC 50844-921 · L.N.K. International, Inc.

FDA lists marketing as ended on 2026-08-31.
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

50844-921-12 — 1 BOTTLE, PLASTIC in 1 CARTON (50844-921-12) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

50844-921-14 — 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-921-14)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50580-933 — Ibuprofen, 50844-257 — Ibuprofen, 50844-291 — ibuprofen, 50844-292 — ibuprofen, 50844-352 — ibuprofen, 50844-353 — ibuprofen, 50844-392 — ibuprofen, 50844-393 — ibuprofen, 50844-438 — ibuprofen, 50844-754 — Ibuprofen, 51013-103 — Ibuprofen, 51013-319 — Ibuprofen, 51013-405 — Ibuprofen, 51013-410 — Ibuprofen, 51013-421 — Ibuprofen, 51013-422 — Ibuprofen, 51013-429 — Ibuprofen, 51316-131 — Acetaminophen and Ibuprofen, 51316-132 — Acetaminophen and Ibuprofen, 51316-187 — 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.