NDC Code | 51662-1343-1 |
Package Description | 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] |