PrednisoLONE - Prednisolone
Navigation: NDC > Supplier starting with: Q > QUALITEST PHARMACEUTICALS| Field | Value |
|---|---|
| NDC Code: | 0603-1567 |
| Proprietary Name: | PrednisoLONE |
| Suffix: | |
| Non-Proprietary Name: | Prednisolone |
| Dosage Form: | SYRUP |
| Method: | ORAL |
| Original Marketing Date: | 21-09-2007 |
| Category Name: | ANDA |
| Application Number: | ANDA040775 |
| Labeler: | QUALITEST PHARMACEUTICALS |
| Substance Name: | PREDNISOLONE |
| Active Numerator Strength: | 15 |
| Active Ingredient Unit: | mg/5mL |
| Pharm Classes: | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
| DEA Schedule: |