| NDC Code | 68084-722-65 |
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| Package Description | 50 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-722-65) > 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-722-11) |
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| Product NDC | 68084-722 |
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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 | 20140319 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA202632 |
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| Manufacturer | American Health Packaging |
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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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