| NDC Code | 65862-884-99 |
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| Package Description | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-884-99) |
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| Product NDC | 65862-884 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Minocycline Hydrochloride |
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| Non-Proprietary Name | Minocycline Hydrochloride |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20160613 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA202261 |
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| Manufacturer | Aurobindo Pharma Limited |
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| Substance Name | MINOCYCLINE HYDROCHLORIDE |
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| Strength | 80 |
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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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