| NDC Code | 76045-212-10 |
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| Package Description | 24 BLISTER PACK in 1 CARTON (76045-212-10) / 1 SYRINGE, GLASS in 1 BLISTER PACK / 1 mL in 1 SYRINGE, GLASS (76045-212-00) |
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| Product NDC | 76045-212 |
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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, EMULSION |
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| Usage | INTRAMUSCULAR; INTRAVENOUS |
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| Start Marketing Date | 20240221 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA209192 |
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| Manufacturer | Fresenius Kabi USA, LLC |
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| Substance Name | DEXAMETHASONE SODIUM PHOSPHATE |
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| Strength | 10 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
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