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Prednisolone Sodium Phosphate
Prednisolone Sodium Phosphate - 65580-251-01 - (prednisolone sodium phosphate)
Drug Information of Prednisolone Sodium Phosphate
| Product NDC: | 65580-251 |
| Proprietary Name: | Prednisolone Sodium Phosphate |
| 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 Prednisolone Sodium Phosphate
| Product NDC: | 65580-251 |
| Labeler Name: | Upstate Pharma, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019157 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20020211 |
Package Information of Prednisolone Sodium Phosphate
| Package NDC: | 65580-251-01 |
| Package Description: | 120 mL in 1 BOTTLE (65580-251-01) |
NDC Information of Prednisolone Sodium Phosphate
| NDC Code | 65580-251-01 |
| Proprietary Name | Prednisolone Sodium Phosphate |
| Package Description | 120 mL in 1 BOTTLE (65580-251-01) |
| Product NDC | 65580-251 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | prednisolone sodium phosphate |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20020211 |
| Marketing Category Name | NDA |
| Labeler Name | Upstate Pharma, LLC |
| Substance Name | PREDNISOLONE SODIUM PHOSPHATE |
| Strength Number | 6.7 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
