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IBUPROFEN

NDC 0363-9611 · WALGREENS

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

0363-9611-01 — 100 TABLET in 1 BOTTLE, PLASTIC (0363-9611-01)

0363-9611-05 — 50 TABLET in 1 BOTTLE, PLASTIC (0363-9611-05)

0363-9611-10 — 1000 TABLET in 1 BOTTLE, PLASTIC (0363-9611-10)

0363-9611-31 — 300 TABLET in 1 BOTTLE, PLASTIC (0363-9611-31)

0363-9611-50 — 500 TABLET in 1 BOTTLE, PLASTIC (0363-9611-50)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0363-5220 — Acetaminophen, Ibuprofen, 0363-6199 — acetaminophen, ibuprofen, 0363-8139 — Ibuprofen, 0363-8574 — Ibuprofen, 0363-8901 — Ibuprofen, 0363-9131 — Acetaminophen and Ibuprofen, 0363-9593 — Ibuprofen, 0363-9594 — IBUPROFEN, 0363-9600 — IBUPROFEN, 0363-9601 — IBUPROFEN, 0363-9612 — IBUPROFEN, 0404-0017 — Ibuprofen, 0472-2002 — Ibuprofen, 0536-1147 — Ibuprofen, 0536-1376 — Acetaminophen and Ibuprofen, 0573-0145 — Ibuprofen, Acetaminophen, 0573-0147 — Ibuprofen, Acetaminophen, 0573-0148 — diphenhydramine HCl, ibuprofen, 0573-0149 — ibuprofen, 0573-0150 — 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.