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Prednisolone
Prednisolone - 58177-910-07 - (Prednisolone)
Drug Information of Prednisolone
| Product NDC: | 58177-910 |
| Proprietary Name: | Prednisolone |
| Non Proprietary Name: | Prednisolone |
| Active Ingredient(s): | 15 mg/5mL & nbsp; Prednisolone |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SYRUP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Prednisolone
| Product NDC: | 58177-910 |
| Labeler Name: | ETHEX Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040364 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20040510 |
Package Information of Prednisolone
| Package NDC: | 58177-910-07 |
| Package Description: | 480 mL in 1 BOTTLE (58177-910-07) |
NDC Information of Prednisolone
| NDC Code | 58177-910-07 |
| Proprietary Name | Prednisolone |
| Package Description | 480 mL in 1 BOTTLE (58177-910-07) |
| Product NDC | 58177-910 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Prednisolone |
| Dosage Form Name | SYRUP |
| Route Name | ORAL |
| Start Marketing Date | 20040510 |
| Marketing Category Name | ANDA |
| Labeler Name | ETHEX Corporation |
| Substance Name | PREDNISOLONE |
| Strength Number | 15 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
