| NDC Code | 66220-017-03 |
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| Package Description | 3 VIAL, SINGLE-USE in 1 CARTON (66220-017-03) > 10 mL in 1 VIAL, SINGLE-USE |
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| Product NDC | 66220-017 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Ethyol |
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| Non-Proprietary Name | Amifostine |
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| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20160801 |
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| End Marketing Date | 20201031 |
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| Marketing Category Name | NDA |
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| Application Number | NDA020221 |
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| Manufacturer | Cumberland Pharmaceuticals Inc. |
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| Substance Name | AMIFOSTINE |
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| Strength | 500 |
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| Strength Unit | mg/10mL |
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| Pharmacy Classes | Cytoprotective Agent [EPC],Free Radical Scavenging Activity [MoA] |
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