| NDC Code | 60687-860-01 |
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| Package Description | 100 BLISTER PACK in 1 CARTON (60687-860-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-860-11) |
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| Product NDC | 60687-860 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Ciprofloxacin |
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| Non-Proprietary Name | Ciprofloxacin Hydrochloride |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20240825 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077859 |
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| Manufacturer | American Health Packaging |
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| Substance Name | CIPROFLOXACIN HYDROCHLORIDE |
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| Strength | 500 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Cytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS] |
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