| NDC Code | 70518-0872-0 |
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| Package Description | 1 mL in 1 VIAL (70518-0872-0) |
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| Product NDC | 70518-0872 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Dexamethasone Sodium Phosphate |
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| Non-Proprietary Name | Dexamethasone Sodium Phosphate |
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| Dosage Form | INJECTION, SOLUTION |
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| Usage | INTRAMUSCULAR; INTRAVENOUS |
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| Start Marketing Date | 20171128 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA084916 |
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| Manufacturer | REMEDYREPACK INC. |
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| Substance Name | DEXAMETHASONE SODIUM PHOSPHATE |
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| Strength | 4 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
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