| NDC Code | 13668-485-01 |
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| Package Description | 100 TABLET in 1 BOTTLE (13668-485-01) |
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| Product NDC | 13668-485 |
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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 |
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| Usage | ORAL |
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| Start Marketing Date | 20150402 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA065156 |
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| Manufacturer | Torrent Pharmaceuticals Limited |
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| Substance Name | MINOCYCLINE HYDROCHLORIDE |
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| Strength | 50 |
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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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