| NDC Code | 0078-0799-75 |
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| Package Description | 1 BOTTLE in 1 CARTON (0078-0799-75) / 7.5 mL in 1 BOTTLE |
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| Product NDC | 0078-0799 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Ciprodex |
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| Non-Proprietary Name | Ciprofloxacin And Dexamethasone |
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| Dosage Form | SUSPENSION/ DROPS |
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| Usage | AURICULAR (OTIC) |
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| Start Marketing Date | 20030804 |
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| Marketing Category Name | NDA |
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| Application Number | NDA021537 |
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| Manufacturer | Novartis Pharmaceuticals Corporation |
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| Substance Name | CIPROFLOXACIN HYDROCHLORIDE; DEXAMETHASONE |
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| Strength | 3; 1 |
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| Strength Unit | mg/mL; mg/mL |
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| Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Cytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS] |
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