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IBUPROFEN

NDC 29485-9291 · Lil' Drug Store Products, Inc.

Generic nameIBUPROFEN 200MG
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

29485-9291-3 — 30 POUCH in 1 BOX (29485-9291-3) / 2 TABLET, FILM COATED in 1 POUCH

29485-9291-5 — 50 POUCH in 1 BOX (29485-9291-5) / 2 TABLET, FILM COATED in 1 POUCH

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

25000-121 — Ibuprofen, 25000-122 — Ibuprofen, 25000-123 — Ibuprofen, 25000-133 — Ibuprofen, 25000-135 — Ibuprofen, 25000-136 — Ibuprofen, 27854-777 — Ibuprofen, 29485-6533 — Advil PM, 29485-6552 — IBUPROFEN Capsule, Liquid-filled, 29485-7008 — Advil PM, 30142-050 — diphenhydramine citrate, ibuprofen, 30142-053 — Ibuprofen, 30142-232 — IBUPROFEN, DIPHENHYDRAMINE HCL, 30142-255 — Ibuprofen, 30142-278 — Ibuprofen and Diphenhydramine Citrate, 30142-281 — Ibuprofen, 30142-402 — ibuprofen, 30142-423 — Ibuprofen and Pseudoephedrine Hydrochloride, 30142-497 — Ibuprofen, 30142-513 — 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.