| NDC Code | 51662-1343-3 |
|---|
| Package Description | 25 POUCH in 1 CASE (51662-1343-3) / 1 VIAL in 1 POUCH (51662-1343-2) / 1 mL in 1 VIAL (51662-1343-1) |
|---|
| Product NDC | 51662-1343 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Dexamethasone Sodium Phosphate |
|---|
| Non-Proprietary Name | Dexamethasone Sodium Phosphate |
|---|
| Dosage Form | INJECTION |
|---|
| Usage | INTRAMUSCULAR; INTRAVENOUS |
|---|
| Start Marketing Date | 20181222 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA087702 |
|---|
| Manufacturer | HF Acquisition Co LLC, DBA HealthFirst |
|---|
| Substance Name | DEXAMETHASONE SODIUM PHOSPHATE |
|---|
| Strength | 10 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
|---|