| NDC Code | 0121-0777-08 |
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| Package Description | 237 mL in 1 BOTTLE (0121-0777-08) |
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| Product NDC | 0121-0777 |
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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 | 20170131 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA078988 |
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| Manufacturer | Pharmaceutical Associates, Inc. |
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| Substance Name | PREDNISOLONE SODIUM PHOSPHATE |
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| Strength | 20 |
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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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