| NDC Code | 67877-438-05 |
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| Package Description | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-438-05) |
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| Product NDC | 67877-438 |
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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, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20160930 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA204453 |
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| Manufacturer | Ascend Laboratories, LLC |
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| Substance Name | MINOCYCLINE HYDROCHLORIDE |
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| Strength | 105 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Tetracycline-class Drug [EPC], Tetracyclines [CS] |
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