| NDC Code | 62756-023-40 |
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| Package Description | 1 VIAL, SINGLE-USE in 1 PACKAGE (62756-023-40) > 4 mL in 1 VIAL, SINGLE-USE |
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| Product NDC | 62756-023 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Topotecan Hydrochloride |
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| Non-Proprietary Name | Topotecan Hydrochloride |
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| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20150902 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA202203 |
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| Manufacturer | Sun Pharmaceutical Industries Limited |
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| Substance Name | TOPOTECAN HYDROCHLORIDE |
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| Strength | 4 |
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| Strength Unit | mg/4mL |
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| Pharmacy Classes | Topoisomerase Inhibitor [EPC],Topoisomerase Inhibitors [MoA] |
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