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Pediapred
Pediapred - 53014-250-01 - (prednisolone sodium phosphate)
Drug Information of Pediapred
| Product NDC: | 53014-250 |
| Proprietary Name: | Pediapred |
| Non Proprietary Name: | prednisolone sodium phosphate |
| Active Ingredient(s): | 6.7 mg/5mL & nbsp; prednisolone sodium phosphate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pediapred
| Product NDC: | 53014-250 |
| Labeler Name: | UCB Manufacturing, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019157 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19860528 |
Package Information of Pediapred
| Package NDC: | 53014-250-01 |
| Package Description: | 120 mL in 1 BOTTLE (53014-250-01) |
NDC Information of Pediapred
| NDC Code | 53014-250-01 |
| Proprietary Name | Pediapred |
| Package Description | 120 mL in 1 BOTTLE (53014-250-01) |
| Product NDC | 53014-250 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | prednisolone sodium phosphate |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 19860528 |
| Marketing Category Name | NDA |
| Labeler Name | UCB Manufacturing, Inc. |
| Substance Name | PREDNISOLONE SODIUM PHOSPHATE |
| Strength Number | 6.7 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
