| NDC Code | 51662-1541-1 |
|---|
| Package Description | 10 mL in 1 VIAL (51662-1541-1) |
|---|
| Product NDC | 51662-1541 |
|---|
| 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 | 20220520 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA210967 |
|---|
| Manufacturer | HF Acquisition Co LLC, DBA HealthFirst |
|---|
| Substance Name | DEXAMETHASONE SODIUM PHOSPHATE |
|---|
| Strength | 100 |
|---|
| Strength Unit | mg/10mL |
|---|
| Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
|---|