NDC 71839-144
Dalbavancin 500 mg per 25 mL injection, powder, lyophilized, for solution
On the label: BE Pharmaceuticals Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Be Biosol Private Limited | Medchal-Malkajgiri, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyNov 12, 2024 · 3 inspections |
Product details
- Generic drug
- Dalbavancin: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous
- Strength
- 500 mg per 25 mL
- Approval
- ANDA ANDA219604
- On the market since
- Jun 12, 2026
- Package NDCs
71839-144-01- Official label
- DailyMed (National Library of Medicine), updated Jun 12, 2026
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