| NDC Code | 63304-296-03 |
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| Package Description | 10 TABLET, FILM COATED in 1 BOTTLE (63304-296-03) |
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| Product NDC | 63304-296 |
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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 | 20090107 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA040766 |
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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 | Antirheumatic Agent [EPC],Antimalarial [EPC] |
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