| NDC Code | 70771-1138-5 |
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| Package Description | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1138-5) |
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| Product NDC | 70771-1138 |
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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, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20180307 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA203553 |
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| Manufacturer | Zydus Lifesciences Limited |
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| Substance Name | MINOCYCLINE HYDROCHLORIDE |
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| Strength | 45 |
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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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