| NDC Code | 0143-9533-01 |
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| Package Description | 1 VIAL in 1 BOX, UNIT-DOSE (0143-9533-01) > 25 mL in 1 VIAL |
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| Product NDC | 0143-9533 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Allopurinol Sodium |
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| Non-Proprietary Name | Allopurinol Sodium |
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| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20040901 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA076870 |
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| Manufacturer | Hikma Pharmaceuticals USA Inc. |
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| Substance Name | ALLOPURINOL SODIUM |
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| Strength | 500 |
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| Strength Unit | mg/25mL |
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| Pharmacy Classes | Xanthine Oxidase Inhibitor [EPC], Xanthine Oxidase Inhibitors [MoA] |
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