| NDC Code | 71337-019-05 |
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| Package Description | 500 TABLET in 1 BOTTLE (71337-019-05) |
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| Product NDC | 71337-019 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Hydroxychloroquine Sulfate |
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| Non-Proprietary Name | Hydroxychloroquine Sulfate |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20200813 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA212902 |
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| Manufacturer | Havix Group Inc d-b-a Aavis Pharmaceuticals |
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| Substance Name | HYDROXYCHLOROQUINE SULFATE |
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| Strength | 200 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Antirheumatic Agent [EPC],Antimalarial [EPC] |
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