NDC 68727-745
Vyxeos 44 mg per 20 mL / 100 mg per 20 mL injection, powder, lyophilized, for suspension
On the label: Jazz Pharmaceuticals, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Jazz Pharmaceuticals Ireland Limited | Athlone, Ireland | Makes it and tests it | Problems found, fixed voluntarilyFeb 24, 2022 · 3 inspections |
| Jazz Pharmaceuticals Ireland Limited | Dublin 4, Ireland | Makes it | Not inspected on record |
| Simtra Deutschland GmbH | Halle/Westfalen, Germany | Makes it, tests it and packages it | Serious problems, FDA actionSep 26, 2025 · 11 inspections, 1 with FDA action |
| Almac Sciences (Ireland) Limited | Athlone, Ireland | Tests it | Problems found, fixed voluntarilyJan 29, 2025 · 4 inspections |
| Charles River Laboratories Ireland Limited | Ballina, Ireland | Tests it | Problems found, fixed voluntarilyMar 31, 2022 · 5 inspections |
| Eurofins Biopharma Product Testing Ireland Limited | Ireland | Tests it | Problems found, fixed voluntarilyMay 26, 2023 · 5 inspections |
| Eurofins Lancaster Laboratories, LLC | Lancaster, PA, United States | Tests it | Problems found, fixed voluntarilyAug 26, 2025 · 8 inspections |
| Millmount Healthcare Limited | Stamullen, Ireland | Packages it and labels it | Problems found, fixed voluntarilyDec 9, 2022 · 3 inspections |
Product details
- Generic drug
- Cytarabine and Daunorubicin: every company that makes it
- Form
- injection, powder, lyophilized, for suspension, intravenous
- Strength
- 44 mg per 20 mL / 100 mg per 20 mL
- Approval
- NDA NDA209401
- On the market since
- Aug 3, 2017
- Package NDCs
68727-745-0168727-745-0268727-745-05- Official label
- DailyMed (National Library of Medicine), updated Jan 30, 2026
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