| NDC Code | 57664-761-13 |
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| Package Description | 500 TABLET in 1 BOTTLE (57664-761-13) |
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| Product NDC | 57664-761 |
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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 | 20180618 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA201691 |
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| Manufacturer | Sun Pharmaceutical Industries, Inc. |
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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 | Antimalarial [EPC], Antirheumatic Agent [EPC] |
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