IBUPROFEN AND FAMOTIDINE
NDC 31722-315 · Camber Pharmaceuticals, Inc.
Generic nameIbuprofen and 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
31722-315-90 — 90 TABLET in 1 BOTTLE (31722-315-90)
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
30142-513 — ibuprofen, 30142-604 — Ibuprofen, 30142-660 — Ibuprofen, 30142-720 — Acetaminophen, Ibuprofen, 30142-743 — Ibuprofen, 30142-745 — Ibuprofen, 30142-965 — Ibuprofen, 31722-017 — Famotidine, 31722-018 — Famotidine, 31722-063 — FAMOTIDINE, 35916-0989 — Ibuprofen, 36800-050 — diphenhydramine citrate and ibuprofen, 36800-057 — ibuprofen, 36800-082 — Famotidine, Calcium Carbonate, Magnesium Hydroxide, 36800-141 — Famotidine, 36800-166 — Ibuprofen, 36800-193 — Ibuprofen, 36800-194 — Famotidine, 36800-221 — Ibuprofen, 36800-237 — IBUPROFEN, DIPHENHYDRAMINE HCL, +1712 more