| NDC Code | 70594-064-02 |
|---|
| Package Description | 10 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (70594-064-02) > 5 mL in 1 VIAL, PHARMACY BULK PACKAGE (70594-064-01) |
|---|
| Product NDC | 70594-064 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Phenylephrine Hydrochloride |
|---|
| Non-Proprietary Name | Phenylephrine Hydrochloride |
|---|
| Dosage Form | INJECTION |
|---|
| Usage | INTRAVENOUS |
|---|
| Start Marketing Date | 20220101 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA213318 |
|---|
| Manufacturer | Xellia Pharmaceuticals USA LLC |
|---|
| Substance Name | PHENYLEPHRINE HYDROCHLORIDE |
|---|
| Strength | 50 |
|---|
| Strength Unit | mg/5mL |
|---|
| Pharmacy Classes | Adrenergic alpha1-Agonists [MoA], alpha-1 Adrenergic Agonist [EPC] |
|---|