| NDC Code | 0093-3165-01 |
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| Package Description | 100 CAPSULE in 1 BOTTLE (0093-3165-01) |
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| Product NDC | 0093-3165 |
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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 | CAPSULE |
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| Usage | ORAL |
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| Start Marketing Date | 19920501 |
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| End Marketing Date | 20180430 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA063011 |
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| Manufacturer | Teva Pharmaceuticals USA, Inc. |
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| Substance Name | MINOCYCLINE HYDROCHLORIDE |
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| Strength | 50 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Tetracycline-class Drug [EPC],Tetracyclines [Chemical/Ingredient] |
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