| NDC Code | 11819-351-30 |
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| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (11819-351-30) |
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| Product NDC | 11819-351 |
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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 | 20040609 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA076794 |
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| Manufacturer | HHS/Program Support Center/Supply Service Center |
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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 | Quinolone Antimicrobial [EPC],Quinolones [CS] |
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