| NDC Code | 70518-1170-0 |
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| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (70518-1170-0) / 5 mL in 1 BOTTLE, PLASTIC |
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| Product NDC | 70518-1170 |
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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 | 20180515 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA019992 |
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| Manufacturer | REMEDYREPACK 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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