| NDC Code | 50742-383-12 |
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| Package Description | 2 BLISTER PACK in 1 CARTON (50742-383-12) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (50742-383-06) |
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| Product NDC | 50742-383 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Prednisolone Sodium Phosphate |
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| Proprietary Name Suffix | Odt |
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| Non-Proprietary Name | Prednisolone Sodium Phosphate |
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| Dosage Form | TABLET, ORALLY DISINTEGRATING |
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| Usage | ORAL |
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| Start Marketing Date | 20250915 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA021959 |
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| Manufacturer | Ingenus Pharmaceuticals, LLC |
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| Substance Name | PREDNISOLONE SODIUM PHOSPHATE |
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| Strength | 10 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
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