| NDC Code | 53942-112-03 |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (53942-112-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC |
| Product NDC | 53942-112 |
| Product Type Name | HUMAN OTC DRUG |
| Proprietary Name | Ibuprofen |
| Non-Proprietary Name | Ibuprofen |
| Dosage Form | TABLET, COATED |
| Usage | ORAL |
| Start Marketing Date | 20250716 |
| Marketing Category Name | ANDA |
| Application Number | ANDA202312 |
| Manufacturer | Demoulas Super Markets, Inc |
| Substance Name | IBUPROFEN |
| Strength | 200 |
| Strength Unit | mg/1 |
| Pharmacy Classes | Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC] |