| NDC Code | 57664-856-85 |
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| Package Description | 50 TABLET, FILM COATED in 1 BOTTLE (57664-856-85) |
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| Product NDC | 57664-856 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Minocycline |
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| Non-Proprietary Name | Minocycline Hydrochloride |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20160129 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA090217 |
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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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