| NDC Code | 72143-223-30 |
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| Package Description | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72143-223-30) |
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| Product NDC | 72143-223 |
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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, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20200420 |
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| End Marketing Date | 20240331 |
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| Marketing Category Name | NDA |
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| Application Number | NDA201922 |
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| Manufacturer | JG Pharma, 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 | Decreased Prothrombin Activity [PE], Tetracycline-class Drug [EPC], Tetracyclines [CS] |
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