NDC 62756-218
Ibandronate Sodium 3 mg per 3 mL injection, solution
On the label: Caraco Pharmaceutical Laboratories, Ltd..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Sun Pharmaceutical Industries Limited | Halol, India | Makes it and tests it | Serious problems, FDA actionJun 13, 2025 · 12 inspections, 5 with FDA action |
Product details
- Generic drug
- Ibandronic Acid: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 3 mg per 3 mL
- Approval
- ANDA ANDA090853
- On the market since
- Feb 15, 2014
- Package NDCs
62756-218-40- Official label
- DailyMed (National Library of Medicine), updated Mar 3, 2026
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