| NDC Code | 70842-160-10 |
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| Package Description | 10 VIAL in 1 CARTON (70842-160-10) / 1 INJECTION in 1 VIAL (70842-160-01) |
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| Product NDC | 70842-160 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Minocin |
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| Non-Proprietary Name | Minocycline Hydrochloride |
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| Dosage Form | INJECTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20130419 |
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| Marketing Category Name | NDA |
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| Application Number | NDA050444 |
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| Manufacturer | Melinta Therapeutics, LLC |
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| Substance Name | MINOCYCLINE HYDROCHLORIDE |
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| Strength | 100 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Decreased Prothrombin Activity [PE], Tetracycline-class Drug [EPC], Tetracyclines [CS] |
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