| NDC Code | 13668-201-01 |
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| Package Description | 100 TABLET in 1 BOTTLE (13668-201-01) |
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| Product NDC | 13668-201 |
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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 |
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| Usage | ORAL |
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| Start Marketing Date | 20140403 |
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| End Marketing Date | 20240531 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA200160 |
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| Manufacturer | Torrent Pharmaceuticals Limited |
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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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