NDC Code | 69238-2122-9 |
Package Description | 237 mL in 1 BOTTLE (69238-2122-9) |
Product NDC | 69238-2122 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Prednisolone Sodium Phosphate |
Non-Proprietary Name | Prednisolone Sodium Phosphate |
Dosage Form | SOLUTION |
Usage | ORAL |
Start Marketing Date | 20221027 |
Marketing Category Name | ANDA |
Application Number | ANDA216715 |
Manufacturer | Amneal Pharmaceuticals NY LLC |
Substance Name | PREDNISOLONE SODIUM PHOSPHATE |
Strength | 15 |
Strength Unit | mg/5mL |
Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |