| NDC Code | 0115-9935-08 |
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| Package Description | 1 BOTTLE in 1 CARTON (0115-9935-08) / 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE |
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| Product NDC | 0115-9935 |
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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 | 20090723 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA050808 |
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| Manufacturer | Amneal Pharmaceuticals of New York, 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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