NDC Code | 0178-0582-01 |
Package Description | 30 mL in 1 BOTTLE (0178-0582-01) |
Product NDC | 0178-0582 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Prednisolone Sodium Phosphate Oral Solution |
Non-Proprietary Name | Prednisolone Sodium Phosphate |
Dosage Form | SOLUTION |
Usage | ORAL |
Start Marketing Date | 20121001 |
Marketing Category Name | ANDA |
Application Number | ANDA091396 |
Manufacturer | Mission Pharmacal Company |
Substance Name | PREDNISOLONE SODIUM PHOSPHATE |
Strength | 25 |
Strength Unit | mg/5mL |
Pharmacy Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |