| NDC Code | 0615-8218-39 |
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| Package Description | 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8218-39) |
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| Product NDC | 0615-8218 |
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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, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20180710 |
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| End Marketing Date | 20210430 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA040104 |
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| Manufacturer | NCS HealthCare of KY, Inc dba Vangard Labs |
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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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