Product NDC: | 0603-9388 |
Proprietary Name: | Prednisolone Sodium Phosphate |
Non Proprietary Name: | Prednisolone Sodium Phosphate |
Active Ingredient(s): | 15 mg/5mL & nbsp; Prednisolone Sodium Phosphate |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0603-9388 |
Labeler Name: | Qualitest Pharmaceuticals |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA079010 |
Marketing Category: | ANDA |
Start Marketing Date: | 20090526 |
Package NDC: | 0603-9388-56 |
Package Description: | 237 mL in 1 BOTTLE (0603-9388-56) |
NDC Code | 0603-9388-56 |
Proprietary Name | Prednisolone Sodium Phosphate |
Package Description | 237 mL in 1 BOTTLE (0603-9388-56) |
Product NDC | 0603-9388 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Prednisolone Sodium Phosphate |
Dosage Form Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 20090526 |
Marketing Category Name | ANDA |
Labeler Name | Qualitest Pharmaceuticals |
Substance Name | PREDNISOLONE SODIUM PHOSPHATE |
Strength Number | 15 |
Strength Unit | mg/5mL |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |