| NDC Code | 0781-6218-70 |
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| Package Description | 1 BOTTLE in 1 CARTON (0781-6218-70) / 10 mL in 1 BOTTLE |
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| Product NDC | 0781-6218 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Ciprofloxacin Hydrochloride And Hydrocortisone |
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| Non-Proprietary Name | Ciprofloxacin Hydrochloride And Hydrocortisone |
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| Dosage Form | SUSPENSION/ DROPS |
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| Usage | AURICULAR (OTIC) |
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| Start Marketing Date | 19990315 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA020805 |
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| Manufacturer | Sandoz Inc |
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| Substance Name | CIPROFLOXACIN HYDROCHLORIDE; HYDROCORTISONE |
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| Strength | 2; 10 |
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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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