| NDC Code | 67877-643-14 |
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| Package Description | 10 BLISTER PACK in 1 CARTON (67877-643-14) / 14 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
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| Product NDC | 67877-643 |
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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 | 65 |
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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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