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Ibuprofen

NDC 11788-010 · AiPing Pharmaceutical, Inc.

Generic nameIbuprofen
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)IBUPROFEN
Strength800 mg/1
Pharmacologic classAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
Marketing categoryANDA

Packages

11788-010-01 — 100 TABLET, FILM COATED in 1 BOTTLE (11788-010-01)

11788-010-05 — 500 TABLET, FILM COATED in 1 BOTTLE (11788-010-05)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

11673-683 — Ibuprofen Mini 200 mg, 11673-685 — Ibuprofen, 11673-741 — ibuprofen, 11673-924 — Acetaminophen, Ibuprofen, 11673-990 — IBUPROFEN, 11673-991 — IBUPROFEN, 11673-992 — IBUPROFEN, 11673-993 — IBUPROFEN, 11788-008 — Ibuprofen, 11788-009 — Ibuprofen, 11822-0050 — Diphenhydramine Citrate, Ibuprofen, 11822-0084 — Ibuprofen and Pseudoephedrine Hydrochloride, 11822-0166 — Ibuprofen, 11822-0231 — Ibuprofen, 11822-0255 — Ibuprofen, 11822-0291 — Ibuprofen, 11822-0292 — Ibuprofen, 11822-0392 — Ibuprofen, 11822-0393 — Ibuprofen, 11822-0589 — 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.