| NDC Code | 82619-131-03 |
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| Package Description | 1000 TABLET in 1 BOTTLE (82619-131-03) |
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| Product NDC | 82619-131 |
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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 | 20250508 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA040150 |
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| Manufacturer | Creekwood Pharmaceuticals LLC |
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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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