| NDC Code | 51662-1660-3 |
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| Package Description | 10 POUCH in 1 CASE (51662-1660-3) / 1 VIAL in 1 POUCH (51662-1660-2) / 5 mL in 1 VIAL (51662-1660-1) |
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| Product NDC | 51662-1660 |
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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 | 19750715 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA084282 |
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| Manufacturer | HF Acquisition Co LLC, DBA HealthFirst |
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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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