| NDC Code | 70954-172-20 |
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| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70954-172-20) |
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| Product NDC | 70954-172 |
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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 | 20220114 |
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| Marketing Category Name | NDA |
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| Application Number | NDA214581 |
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| Manufacturer | ANI Pharmaceuticals, 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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