| NDC Code | 55111-422-30 |
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| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-422-30) |
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| Product NDC | 55111-422 |
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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, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20070326 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077902 |
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| Manufacturer | Dr. Reddy's Laboratories Limited |
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| Substance Name | CIPROFLOXACIN HYDROCHLORIDE; CIPROFLOXACIN |
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| Strength | 287.5; 212.6 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Quinolone Antimicrobial [EPC],Quinolones [CS],Quinolone Antimicrobial [EPC],Quinolones [CS] |
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