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PrednisoLONE
PrednisoLONE - 0603-1567-56 - (Prednisolone)
Drug Information of PrednisoLONE
| 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) |
Labeler Information of PrednisoLONE
| 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 Information of PrednisoLONE
| Package NDC: | 0603-1567-56 |
| Package Description: | 240 mL in 1 BOTTLE (0603-1567-56) |
NDC Information of PrednisoLONE
| NDC Code | 0603-1567-56 |
| Proprietary Name | PrednisoLONE |
| Package Description | 240 mL in 1 BOTTLE (0603-1567-56) |
| 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] |
