| NDC Code | 50419-754-01 |
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| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50419-754-01) |
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| Product NDC | 50419-754 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Cipro |
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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 | 19871022 |
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| Marketing Category Name | NDA |
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| Application Number | NDA019537 |
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| Manufacturer | Bayer HealthCare Pharmaceuticals Inc. |
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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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