| NDC Code | 50090-2313-3 |
|---|
| Package Description | 1 mL in 1 VIAL (50090-2313-3) |
|---|
| Product NDC | 50090-2313 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Dexamethasone Sodium Phosphate |
|---|
| Non-Proprietary Name | Dexamethasone Sodium Phosphate |
|---|
| Dosage Form | INJECTION, SOLUTION |
|---|
| Usage | INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; INTRAVENOUS; SOFT TISSUE |
|---|
| Start Marketing Date | 20110511 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA040803 |
|---|
| Manufacturer | A-S Medication Solutions |
|---|
| Substance Name | DEXAMETHASONE SODIUM PHOSPHATE |
|---|
| Strength | 4 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
|---|