| NDC Code | 0641-6229-25 |
|---|
| Package Description | 25 VIAL in 1 CARTON (0641-6229-25) / 1 mL in 1 VIAL (0641-6229-01) |
|---|
| Product NDC | 0641-6229 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Phenylephrine Hydrochloride |
|---|
| Non-Proprietary Name | Phenylephrine Hydrochloride |
|---|
| Dosage Form | INJECTION |
|---|
| Usage | INTRAVENOUS |
|---|
| Start Marketing Date | 20121218 |
|---|
| Marketing Category Name | NDA |
|---|
| Application Number | NDA203826 |
|---|
| Manufacturer | Hikma Pharmaceuticals USA Inc. |
|---|
| Substance Name | PHENYLEPHRINE HYDROCHLORIDE |
|---|
| Strength | 10 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Adrenergic alpha1-Agonists [MoA], alpha-1 Adrenergic Agonist [EPC] |
|---|