| NDC Code | 13913-001-30 |
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| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (13913-001-30) |
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| Product NDC | 13913-001 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Proquin |
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| Proprietary Name Suffix | Xr |
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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 | 20051001 |
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| Marketing Category Name | NDA |
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| Application Number | NDA021744 |
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| Manufacturer | Depomed, 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 | Quinolone Antimicrobial [EPC],Quinolones [CS] |
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