| NDC Code | 62037-942-06 |
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| Package Description | 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-942-06) |
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| Product NDC | 62037-942 |
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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 |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20101130 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077417 |
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| Manufacturer | Watson Pharma, Inc. |
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| Substance Name | CIPROFLOXACIN; CIPROFLOXACIN HYDROCHLORIDE |
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| Strength | 212.6; 287.5 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient],Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |
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