| NDC Code | 41250-050-58 |
|---|
| Package Description | 1 BOTTLE in 1 CARTON (41250-050-58) / 40 TABLET, FILM COATED in 1 BOTTLE |
|---|
| Product NDC | 41250-050 |
|---|
| 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 | 20090408 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA079113 |
|---|
| Manufacturer | Meijer Distribution Inc |
|---|
| 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] |
|---|