| NDC Code | 71384-512-01 |
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| Package Description | 20 VIAL, SINGLE-USE in 1 BOX (71384-512-01) > 1 mL in 1 VIAL, SINGLE-USE |
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| Product NDC | 71384-512 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Dex-moxi |
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| Non-Proprietary Name | Dexamethasone Phosphate - Moxifloxacin |
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| Dosage Form | INJECTION, SOLUTION |
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| Usage | OPHTHALMIC |
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| Start Marketing Date | 20180105 |
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| Marketing Category Name | UNAPPROVED DRUG OTHER |
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| Manufacturer | Imprimis NJOF, LLC |
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| Substance Name | DEXAMETHASONE SODIUM PHOSPHATE; MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE |
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| Strength | 1; 5 |
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| Strength Unit | mg/mL; mg/mL |
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| Pharmacy Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Quinolone Antimicrobial [EPC],Quinolones [CS] |
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