NDC 65862-942
Levalbuterol 1.25 mg per 0.5 mL solution, concentrate
On the label: Aurobindo Pharma Limited.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aarti Pharmalabs Limited | Tarapur, India | Makes the active ingredient | Problems found, fixed voluntarilyMar 27, 2026 · 5 inspections |
| Eugia Pharma Specialities Limited | Sangareddy, India | Makes it and tests it | Serious problems, FDA actionFeb 6, 2026 · 7 inspections, 2 with FDA action |
Product details
- Generic drug
- Levalbuterol: every company that makes it
- Form
- solution, concentrate, respiratory (inhalation)
- Strength
- 1.25 mg per 0.5 mL
- Approval
- ANDA ANDA207628
- On the market since
- Jan 31, 2017
- Package NDCs
65862-942-0365862-942-50- Official label
- DailyMed (National Library of Medicine), updated Oct 31, 2023
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