| NDC Code | 10631-332-05 |
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| Package Description | 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (10631-332-05) |
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| Product NDC | 10631-332 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Ximino |
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| Non-Proprietary Name | Minocycline Hydrochloride |
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| Dosage Form | CAPSULE, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20171025 |
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| Marketing Category Name | NDA |
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| Application Number | NDA201922 |
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| Manufacturer | Sun Pharmaceutical Industries, Inc |
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| Substance Name | MINOCYCLINE HYDROCHLORIDE |
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| Strength | 135 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Tetracycline-class Drug [EPC],Tetracyclines [CS] |
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