| NDC Code | 17856-0759-5 |
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| Package Description | 5 mL in 1 CUP (17856-0759-5) |
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| Product NDC | 17856-0759 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Prednisolone Sodium Phosphate |
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| Non-Proprietary Name | Prednisolone Sodium Phosphate |
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| Dosage Form | SOLUTION |
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| Usage | ORAL |
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| Start Marketing Date | 20050425 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA076913 |
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| Manufacturer | Atlantic Biologicals Corps. |
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| Substance Name | PREDNISOLONE SODIUM PHOSPHATE |
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| Strength | 15 |
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| Strength Unit | mg/5mL |
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| Pharmacy Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
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