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Prednisolone Sodium Phosphate
Prednisolone Sodium Phosphate - 0121-0759-08 - (Prednisolone Sodium Phosphate)
Drug Information of Prednisolone Sodium Phosphate
| Product NDC: | 0121-0759 |
| 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) |
Labeler Information of Prednisolone Sodium Phosphate
| Product NDC: | 0121-0759 |
| Labeler Name: | Pharmaceutical Associates, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076913 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20050425 |
Package Information of Prednisolone Sodium Phosphate
| Package NDC: | 0121-0759-08 |
| Package Description: | 237 mL in 1 BOTTLE (0121-0759-08) |
NDC Information of Prednisolone Sodium Phosphate
| NDC Code | 0121-0759-08 |
| Proprietary Name | Prednisolone Sodium Phosphate |
| Package Description | 237 mL in 1 BOTTLE (0121-0759-08) |
| Product NDC | 0121-0759 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Prednisolone Sodium Phosphate |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20050425 |
| Marketing Category Name | ANDA |
| Labeler Name | Pharmaceutical Associates, Inc. |
| Substance Name | PREDNISOLONE SODIUM PHOSPHATE |
| Strength Number | 15 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
