| NDC Code | 42852-001-02 |
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| Package Description | 20 TABLET in 1 BOTTLE, PLASTIC (42852-001-02) |
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| Product NDC | 42852-001 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Ciprofloxacin Hydrochloride |
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| Non-Proprietary Name | Ciprofloxacin Hydrochloride |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20110701 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA075593 |
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| Manufacturer | Apothecary Shop Wholesale 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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