Ibuprofen Famotidine
NDC 72189-667 · Direct_Rx
Generic nameIbuprofen Famotidine
Dosage formTABLET
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
72189-667-90 — 90 TABLET in 1 BOTTLE (72189-667-90)
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
72189-141 — FAMOTIDINE, 72189-207 — FAMOTIDINE, 72189-231 — IBUPROFEN, 72189-266 — IBUPROFEN, 72189-324 — IBUPROFEN, 72189-543 — Famotidine, 72189-556 — Ibuprofen, 72189-564 — Ibuprofen, 72189-641 — Ibuprofen Famotidine, 72189-643 — Ibuprofen, 72205-145 — Famotidine, 72205-146 — Famotidine, 72205-233 — FAMOTIDINE, 72260-129 — ACETAMINOPHEN and IBUPROFEN, 72288-050 — diphenhydramine citrate, ibuprofen, 72288-057 — ibuprofen, 72288-061 — Ibuprofen and Diphenhydramine Citrate, 72288-080 — Ibuprofen, 72288-131 — Ibuprofen, 72288-141 — Famotidine, +1712 more