| NDC Code | 63548-0197-8 |
|---|
| Package Description | 8 TABLET in 1 BOTTLE, PLASTIC (63548-0197-8) |
|---|
| Product NDC | 63548-0197 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Ibuprofen 200 Mg And Diphenhydramine Citrate 38 Mg |
|---|
| Non-Proprietary Name | Ibuprofen, Diphenhydramine Citrate |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20240411 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA211404 |
|---|
| Manufacturer | PLD Acquisitions LLC DBA Av�ma Pharma Solutions |
|---|
| 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] |
|---|