| NDC Code | 50419-788-00 |
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| Package Description | 38220 TABLET, FILM COATED, EXTENDED RELEASE in 1 DRUM (50419-788-00) |
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| Product NDC | 50419-788 |
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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 |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20121001 |
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| Marketing Category Name | NDA |
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| Application Number | NDA021473 |
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| Manufacturer | Bayer HealthCare Pharmaceuticals 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; 1/1 |
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| Pharmacy Classes | Quinolone Antimicrobial [EPC],Quinolones [CS],Quinolone Antimicrobial [EPC],Quinolones [CS] |
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