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IBUPROFEN

NDC 11822-7892 · RITE AID CORPORATION

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

11822-7892-0 — 24 TABLET, COATED in 1 BOTTLE (11822-7892-0)

11822-7892-2 — 50 TABLET, COATED in 1 BOTTLE (11822-7892-2)

11822-7892-5 — 100 TABLET, COATED in 1 BOTTLE (11822-7892-5)

11822-7892-7 — 200 TABLET, COATED in 1 BOTTLE (11822-7892-7)

11822-7892-9 — 500 TABLET, COATED in 1 BOTTLE (11822-7892-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

11822-1131 — Acetaminophen and Ibuprofen (NSAID), 11822-1521 — Ibuprofen, 11822-1685 — Ibuprofen, 11822-1879 — Ibuprofen, 11822-3307 — Ibuprofen, 11822-4258 — Ibuprofen, 11822-4461 — Ibuprofen, 11822-5777 — Acetaminophen, Ibuprofen, 11822-6604 — Ibuprofen, 11822-7891 — IBUPROFEN, 11822-7893 — IBUPROFEN, 11822-8925 — IBUPROFEN, 11822-9998 — Ibuprofen, 13107-004 — Hydrocodone Bitartrate and Ibuprofen, 17856-5309 — Ibuprofen, 17856-5310 — Ibuprofen, 21130-006 — Ibuprofen, 21130-032 — Ibuprofen, 21130-056 — Diphenhydramine Citrate, Ibuprofen, 21130-070 — 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.