| NDC Code | 43063-585-10 |
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| Package Description | 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-585-10) |
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| Product NDC | 43063-585 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Moxifloxacin Hydrochloride |
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| Non-Proprietary Name | Moxifloxacin Hydrochloride |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20140129 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA021085 |
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| Manufacturer | PD-Rx Pharmaceuticals, Inc. |
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| Substance Name | MOXIFLOXACIN HYDROCHLORIDE |
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| Strength | 400 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Quinolone Antimicrobial [EPC],Quinolones [CS] |
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