Product NDC: | 0603-1567 |
Proprietary Name: | PrednisoLONE |
Non Proprietary Name: | Prednisolone |
Active Ingredient(s): | 15 mg/5mL & nbsp; Prednisolone |
Administration Route(s): | ORAL |
Dosage Form(s): | SYRUP |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0603-1567 |
Labeler Name: | Qualitest Pharmaceuticals |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040775 |
Marketing Category: | ANDA |
Start Marketing Date: | 20070921 |
Package NDC: | 0603-1567-58 |
Package Description: | 480 mL in 1 BOTTLE (0603-1567-58) |
NDC Code | 0603-1567-58 |
Proprietary Name | PrednisoLONE |
Package Description | 480 mL in 1 BOTTLE (0603-1567-58) |
Product NDC | 0603-1567 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Prednisolone |
Dosage Form Name | SYRUP |
Route Name | ORAL |
Start Marketing Date | 20070921 |
Marketing Category Name | ANDA |
Labeler Name | Qualitest Pharmaceuticals |
Substance Name | PREDNISOLONE |
Strength Number | 15 |
Strength Unit | mg/5mL |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |