| NDC Code | 50580-436-01 |
|---|
| Package Description | 2 BLISTER PACK in 1 CARTON (50580-436-01) / 10 TABLET, FILM COATED in 1 BLISTER PACK |
|---|
| Product NDC | 50580-436 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Sudafed Pe Head Congestion Plus Pain |
|---|
| Non-Proprietary Name | Ibuprofen And Phenylephrine Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20190617 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA203200 |
|---|
| Manufacturer | Johnson & Johnson Consumer Inc. |
|---|
| Substance Name | IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE |
|---|
| Strength | 200; 10 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Adrenergic alpha1-Agonists [MoA], Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC], alpha-1 Adrenergic Agonist [EPC] |
|---|