| NDC Code | 51662-1576-1 |
|---|
| Package Description | 1 mL in 1 VIAL, SINGLE-DOSE (51662-1576-1) |
|---|
| Product NDC | 51662-1576 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Phenylephrine Hydrochloride |
|---|
| Non-Proprietary Name | Phenylephrine Hydrochloride |
|---|
| Dosage Form | INJECTION |
|---|
| Usage | INTRAVENOUS |
|---|
| Start Marketing Date | 20210630 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA210665 |
|---|
| Manufacturer | HF Acquisition Co LLC, DBA HealthFirst |
|---|
| Substance Name | PHENYLEPHRINE HYDROCHLORIDE |
|---|
| Strength | 10 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Adrenergic alpha1-Agonists [MoA], alpha-1 Adrenergic Agonist [EPC] |
|---|