NDC 23155-170
Zoledronic acid 4 mg per 5 mL injection, solution, concentrate
On the label: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Emcure Pharmaceuticals Limited | Ahmedabad, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyMay 15, 2026 · 3 inspections |
Product details
- Generic drug
- Zoledronic Acid: every company that makes it
- Form
- injection, solution, concentrate, intravenous
- Strength
- 4 mg per 5 mL
- Approval
- ANDA ANDA201783
- On the market since
- Aug 31, 2023
- Package NDCs
23155-170-31- Official label
- DailyMed (National Library of Medicine), updated Sep 18, 2023
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