| NDC Code | 99207-462-30 |
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| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (99207-462-30) |
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| Product NDC | 99207-462 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Solodyn |
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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 | 20060508 |
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| End Marketing Date | 20140228 |
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| Marketing Category Name | NDA |
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| Application Number | NDA050808 |
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| Manufacturer | Medicis Pharmaceutical Corp. |
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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 | Tetracycline-class Drug [EPC],Tetracyclines [Chemical/Ingredient] |
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