NDC 55150-191
Ibandronate Sodium 3 mg per 3 mL injection, solution
On the label: AuroMedics Pharma LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Apitoria Pharma Private Limited | Srikakulam, India | Makes the active ingredient and tests it | No problems foundSep 11, 2026 · 7 inspections, 1 with FDA action |
| Eugia Pharma Specialities Limited | Sangareddy, India | Makes it, tests it and packages it | Serious problems, FDA actionFeb 6, 2026 · 7 inspections, 2 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 ANDA205332
- On the market since
- Aug 19, 2015
- Package NDCs
55150-191-83- Official label
- DailyMed (National Library of Medicine), updated Jan 27, 2026
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