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Ibuprofen

NDC 37808-609 · HEB

Generic nameIbuprofen
Dosage formCAPSULE, LIQUID FILLED
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

37808-609-11 — 1 BOTTLE in 1 CARTON (37808-609-11) / 20 CAPSULE, LIQUID FILLED in 1 BOTTLE

37808-609-78 — 1 BOTTLE in 1 CARTON (37808-609-78) / 80 CAPSULE, LIQUID FILLED in 1 BOTTLE

37808-609-83 — 300 CAPSULE, LIQUID FILLED in 1 BOTTLE (37808-609-83)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

36800-993 — Ibuprofen, 37808-023 — Ibuprofen, 37808-057 — ibuprofen, 37808-109 — Ibuprofen, 37808-200 — Ibuprofen, 37808-255 — Ibuprofen, 37808-363 — Ibuprofen, 37808-393 — Ibuprofen, 37808-410 — Ibuprofen, 37808-604 — Ibuprofen, 37808-647 — Ibuprofen, 37808-699 — Ibuprofen, 37808-703 — diphenhydramine citrate, ibuprofen, 37808-709 — Ibuprofen, 37808-921 — Ibuprofen, 37808-922 — Ibuprofen, 37835-581 — Ibuprofen, 37835-585 — Ibuprofen, 37835-588 — Ibuprofen, 41163-050 — 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.