| NDC Code | 51991-942-98 |
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| Package Description | 1 VIAL, SINGLE-DOSE in 1 CARTON (51991-942-98) / 50 mL in 1 VIAL, SINGLE-DOSE |
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| Product NDC | 51991-942 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Dexrazoxane |
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| Non-Proprietary Name | Dexrazoxane Hydrochloride |
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| Dosage Form | INJECTION, SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20161205 |
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| End Marketing Date | 20240831 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA207321 |
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| Manufacturer | Breckenridge Pharmaceutical, Inc. |
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| Substance Name | DEXRAZOXANE HYDROCHLORIDE |
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| Strength | 500 |
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| Strength Unit | mg/50mL |
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| Pharmacy Classes | Cytoprotective Agent [EPC] |
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