| NDC Code | 0703-5075-01 |
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| Package Description | 1 VIAL, SINGLE-DOSE in 1 CARTON (0703-5075-01) / 20 mL in 1 VIAL, SINGLE-DOSE |
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| Product NDC | 0703-5075 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Dacarbazine |
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| Non-Proprietary Name | Dacarbazine |
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| Dosage Form | INJECTION, POWDER, FOR SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 19980827 |
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| End Marketing Date | 20240531 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA075259 |
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| Manufacturer | Teva Parenteral Medicines, Inc. |
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| Substance Name | DACARBAZINE |
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| Strength | 200 |
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| Strength Unit | mg/20mL |
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| Pharmacy Classes | Alkylating Activity [MoA], Alkylating Drug [EPC] |
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