| NDC Code | 57664-853-85 |
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| Package Description | 50 CAPSULE in 1 BOTTLE (57664-853-85) |
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| Product NDC | 57664-853 |
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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 | CAPSULE |
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| Usage | ORAL |
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| Start Marketing Date | 20130513 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA090867 |
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| Manufacturer | Sun Pharmaceutical Industries, Inc. |
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| Substance Name | MINOCYCLINE HYDROCHLORIDE |
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| Strength | 100 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Tetracycline-class Drug [EPC], Tetracyclines [CS] |
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