Product NDC: | 55154-3276 |
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: | 55154-3276 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA076895 |
Marketing Category: | ANDA |
Start Marketing Date: | 20041004 |
Package NDC: | 55154-3276-4 |
Package Description: | 30 POUCH in 1 CARTON (55154-3276-4) > 5 mL in 1 POUCH (55154-3276-6) |
NDC Code | 55154-3276-4 |
Proprietary Name | Prednisolone Sodium Phosphate |
Package Description | 30 POUCH in 1 CARTON (55154-3276-4) > 5 mL in 1 POUCH (55154-3276-6) |
Product NDC | 55154-3276 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | PREDNISOLONE SODIUM PHOSPHATE |
Dosage Form Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 20041004 |
Marketing Category Name | ANDA |
Labeler Name | Cardinal Health |
Substance Name | PREDNISOLONE SODIUM PHOSPHATE |
Strength Number | 15 |
Strength Unit | mg/5mL |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |