NDC Code | 37012-050-27 |
Package Description | 1 BOTTLE in 1 CARTON (37012-050-27) > 80 TABLET, FILM COATED in 1 BOTTLE |
Product NDC | 37012-050 |
Product Type Name | HUMAN OTC DRUG |
Proprietary Name | Ibuprofen Pm |
Non-Proprietary Name | Diphenhydramine Citrate, Ibuprofen |
Dosage Form | TABLET, FILM COATED |
Usage | ORAL |
Start Marketing Date | 20160803 |
Marketing Category Name | ANDA |
Application Number | ANDA079113 |
Manufacturer | Shopko Stores Operating Co., LLC |
Substance Name | DIPHENHYDRAMINE CITRATE; IBUPROFEN |
Strength | 38; 200 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], Nonsteroidal Anti-inflammatory Drug [EPC] |