| NDC Code | 17856-8815-1 |
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| Package Description | 50 CUP, UNIT-DOSE in 1 CASE (17856-8815-1) / 5 mL in 1 CUP, UNIT-DOSE |
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| Product NDC | 17856-8815 |
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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 | 20231009 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA203559 |
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| Manufacturer | Atlantic Biologicals Corp |
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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 Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
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