| NDC Code | 70518-0359-0 |
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| Package Description | 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0359-0) |
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| Product NDC | 70518-0359 |
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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 |
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| Usage | ORAL |
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| Start Marketing Date | 20170427 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA065436 |
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| Manufacturer | REMEDYREPACK 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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