| NDC Code | 68001-651-37 |
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| Package Description | 1 VIAL, SINGLE-USE in 1 CARTON (68001-651-37) / 20 mL in 1 VIAL, SINGLE-USE |
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| Product NDC | 68001-651 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Paclitaxel Protein-bound Particles For Injectable Suspension (albumin-bound) |
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| Non-Proprietary Name | Paclitaxel |
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| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SUSPENSION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20250611 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA216355 |
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| Manufacturer | BluePoint Laboratories |
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| Substance Name | PACLITAXEL |
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| Strength | 100 |
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| Strength Unit | mg/20mL |
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| Pharmacy Classes | Microtubule Inhibition [PE], Microtubule Inhibitor [EPC] |
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