| NDC Code | 68071-3351-3 |
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| Package Description | 10 mL in 1 BOX (68071-3351-3) |
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| Product NDC | 68071-3351 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Ciprofloxacin Hydrochloride |
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| Non-Proprietary Name | Ciprofloxacin Hydrochloride |
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| Dosage Form | SOLUTION/ DROPS |
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| Usage | OPHTHALMIC |
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| Start Marketing Date | 20040507 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA019992 |
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| Manufacturer | NuCare Pharmaceuticals,Inc. |
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| Substance Name | CIPROFLOXACIN HYDROCHLORIDE |
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| Strength | 3 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Cytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS] |
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