Ibuprofen and famotidine
NDC 59651-908 · Aurobindo Pharma Limited
Generic nameIbuprofen and famotidine
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)IBUPROFEN, FAMOTIDINE
Strength26.6; 800 mg/1; mg/1
Pharmacologic classAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC], Nonsteroidal Anti-inflammatory Drug [EPC]
Marketing categoryANDA
Packages
59651-908-90 — 90 TABLET, FILM COATED in 1 BOTTLE (59651-908-90)
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
59556-858 — IBUPROFEN, 59556-895 — IBUPROFEN, 59640-001 — famotidine, 59640-020 — IBUPROFEN, DIPHENHYDRAMINE HCL, 59640-023 — famotidine, 59651-032 — Ibuprofen Oral, 59651-360 — Ibuprofen, 59651-361 — Ibuprofen, 59651-362 — Ibuprofen, 59651-701 — FAMOTIDINE, 59726-003 — Ibuprofen, 59726-046 — Ibuprofen, 59726-123 — Ibuprofen, 59726-139 — Ibuprofen, 59726-279 — Ibuprofen, 59726-745 — Ibuprofen, 59726-843 — Ibuprofen, 59779-050 — diphenhydramine citrate and ibuprofen, 59779-141 — Famotidine, 59779-166 — Ibuprofen, +1712 more