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Veripred 20
Veripred 20 - 63717-915-08 - (PREDNISOLONE SODIUM PHOSPHATE)
Drug Information of Veripred 20
| Product NDC: | 63717-915 |
| Proprietary Name: | Veripred 20 |
| Non Proprietary Name: | PREDNISOLONE SODIUM PHOSPHATE |
| Active Ingredient(s): | 20 mg/5mL & nbsp; PREDNISOLONE SODIUM PHOSPHATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Veripred 20
| Product NDC: | 63717-915 |
| Labeler Name: | Hawthorne Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078988 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091101 |
Package Information of Veripred 20
| Package NDC: | 63717-915-08 |
| Package Description: | 237 mL in 1 BOTTLE (63717-915-08) |
NDC Information of Veripred 20
| NDC Code | 63717-915-08 |
| Proprietary Name | Veripred 20 |
| Package Description | 237 mL in 1 BOTTLE (63717-915-08) |
| Product NDC | 63717-915 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | PREDNISOLONE SODIUM PHOSPHATE |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20091101 |
| Marketing Category Name | ANDA |
| Labeler Name | Hawthorne Pharmaceuticals, Inc. |
| Substance Name | PREDNISOLONE SODIUM PHOSPHATE |
| Strength Number | 20 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
