ibuprofen
NDC 37808-604 · H E B
Generic nameIbuprofen
Dosage formTABLET, FILM 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
37808-604-71 — 1 BOTTLE in 1 CARTON (37808-604-71) / 50 TABLET, FILM COATED in 1 BOTTLE
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
36800-811 — ibuprofen, 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, 37808-609 — 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, +1311 more