| NDC Code | 70069-022-25 |
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| Package Description | 25 VIAL, SINGLE-DOSE in 1 CARTON (70069-022-25) / 1 mL in 1 VIAL, SINGLE-DOSE (70069-022-01) |
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| Product NDC | 70069-022 |
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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 |
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| Usage | INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; INTRAVENOUS; SOFT TISSUE |
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| Start Marketing Date | 20180608 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA207521 |
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| Manufacturer | Somerset Therapeutics, LLC |
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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 Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
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