| NDC Code | 69367-387-50 |
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| Package Description | 50 TABLET, FILM COATED in 1 BOTTLE (69367-387-50) |
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| Product NDC | 69367-387 |
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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 | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20240523 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA076593 |
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| Manufacturer | Westminster Pharmaceuticals, LLC |
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| Substance Name | CIPROFLOXACIN HYDROCHLORIDE |
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| Strength | 750 |
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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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