| NDC Code | 50268-576-13 |
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| Package Description | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-576-13) > 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-576-11) |
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| Product NDC | 50268-576 |
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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 | 20160722 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA202632 |
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| Manufacturer | AvPAK |
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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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