| NDC Code | 70069-081-01 |
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| Package Description | 1 BOTTLE in 1 CARTON (70069-081-01) / 3 mL in 1 BOTTLE |
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| Product NDC | 70069-081 |
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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 | SOLUTION/ DROPS |
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| Usage | OPHTHALMIC |
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| Start Marketing Date | 20241125 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA209698 |
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| Manufacturer | Somerset Therapeutics, LLC |
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| Substance Name | MOXIFLOXACIN HYDROCHLORIDE |
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| Strength | 5 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS] |
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