| NDC Code | 70934-042-20 |
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| Package Description | 20 CAPSULE in 1 BOTTLE, PLASTIC (70934-042-20) |
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| Product NDC | 70934-042 |
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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 | 20171030 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA065062 |
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| Manufacturer | Denton Pharma, Inc. DBA Northwind Pharmaceuticals |
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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 | Tetracycline-class Drug [EPC], Tetracyclines [CS] |
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