| NDC Code | 0378-4715-22 |
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| Package Description | 48 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (0378-4715-22) |
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| Product NDC | 0378-4715 |
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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 |
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| Dosage Form | TABLET, ORALLY DISINTEGRATING |
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| Usage | ORAL |
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| Start Marketing Date | 20141208 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA202179 |
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| Manufacturer | Mylan Pharmaceuticals Inc. |
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| Substance Name | PREDNISOLONE SODIUM PHOSPHATE |
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| Strength | 15 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
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