Prednisolone Sodium Phosphate - Prednisolone Sodium Phosphate
Navigation: NDC > Supplier starting with: P > PHARMACEUTICAL ASSOCIATES, INC.| Field | Value |
|---|---|
| NDC Code: | 0121-0759 |
| Proprietary Name: | Prednisolone Sodium Phosphate |
| Suffix: | |
| Non-Proprietary Name: | Prednisolone Sodium Phosphate |
| Dosage Form: | SOLUTION |
| Method: | ORAL |
| Original Marketing Date: | 25-04-2005 |
| Category Name: | ANDA |
| Application Number: | ANDA076913 |
| Labeler: | PHARMACEUTICAL ASSOCIATES, INC. |
| Substance Name: | PREDNISOLONE SODIUM PHOSPHATE |
| Active Numerator Strength: | 15 |
| Active Ingredient Unit: | mg/5mL |
| Pharm Classes: | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
| DEA Schedule: |