| NDC Code | 0378-4730-22 |
|---|
| Package Description | 48 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (0378-4730-22) |
|---|
| Product NDC | 0378-4730 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Prednisolone Sodium Phosphate |
|---|
| Non-Proprietary Name | Prednisolone |
|---|
| Dosage Form | TABLET, ORALLY DISINTEGRATING |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20141208 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA202179 |
|---|
| Manufacturer | Mylan Pharmaceuticals Inc. |
|---|
| Substance Name | PREDNISOLONE SODIUM PHOSPHATE |
|---|
| Strength | 30 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
|---|