Ibuprofen
NDC 73614-201 · Brisk Pharmaceuticals
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
73614-201-03 — 30 TABLET, FILM COATED in 1 BOTTLE (73614-201-03)
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
72789-584 — Ibuprofen, 72888-479 — Ibuprofen, 73086-210 — ibuprofen, 73086-211 — ibuprofen, 73086-212 — ibuprofen, 73097-028 — IBUPROFEN, 73408-509 — Ibuprofen, 73408-809 — Ibuprofen, 73598-1102 — IBUPROFEN, 73598-1104 — IBUPROFEN, 75907-158 — Acetaminophen and Ibuprofen (NSAID) Tablets, 250 mg/ 125 mg, 75907-428 — Ibuprofen, 76162-501 — Acetaminophen, Ibuprofen, 76162-520 — acetaminophen, ibuprofen, 76281-119 — IBUPROFEN, 76281-126 — IBUPROFEN, 76281-128 — IBUPROFEN, 76282-712 — Ibuprofen, 76282-713 — Ibuprofen, 76282-714 — Ibuprofen, +1311 more