NDC 72893-002
Beleodaq 500 mg per 10 mL injection, powder, lyophilized, for solution
On the label: Acrotech Biopharma Inc.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Cenexi - Laboratoires Thissen Sa | Braine l'Alleud, Belgium | Makes it and tests it | Problems found, fixed voluntarilyJun 1, 2023 · 8 inspections |
| Curia New York, Inc. | Rensselaer, NY, United States | Makes the active ingredient and tests it | Serious problems, FDA actionFeb 5, 2026 · 8 inspections, 1 with FDA action |
| AndersonBrecon Inc. | Rockford, IL, United States | Packages it and labels it | No problems foundMay 8, 2025 · 6 inspections |
Product details
- Generic drug
- Belinostat: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous
- Strength
- 500 mg per 10 mL
- Approval
- NDA NDA206256
- On the market since
- Jul 21, 2014
- Package NDCs
72893-002-01- Official label
- DailyMed (National Library of Medicine), updated Apr 7, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?