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Ibuprofen

NDC 37808-109 · HEB

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

37808-109-03 — 1 BOTTLE, PLASTIC in 1 CARTON (37808-109-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC

37808-109-08 — 250 TABLET, COATED in 1 BOTTLE, PLASTIC (37808-109-08)

37808-109-10 — 2 BOTTLE, PLASTIC in 1 CARTON (37808-109-10) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

36800-604 — Ibuprofen, 36800-647 — Ibuprofen, 36800-660 — Ibuprofen, 36800-662 — Ibuprofen, 36800-663 — Ibuprofen, 36800-756 — IBUPROFEN, DIPHENHYDRAMINE HCL, 36800-811 — ibuprofen, 36800-993 — Ibuprofen, 37808-023 — Ibuprofen, 37808-057 — ibuprofen, 37808-200 — Ibuprofen, 37808-255 — Ibuprofen, 37808-363 — Ibuprofen, 37808-393 — Ibuprofen, 37808-410 — Ibuprofen, 37808-604 — Ibuprofen, 37808-609 — Ibuprofen, 37808-647 — Ibuprofen, 37808-699 — Ibuprofen, 37808-703 — diphenhydramine citrate, 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.