NDC 50742-393
Albuterol Sulfate 1.25 mg per 3 mL solution
On the label: Ingenus Pharmaceuticals, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lexenpharm (Suzhou) Limited | Suzhou, China | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilySep 4, 2025 · 1 inspection |
Product details
- Generic drug
- Albuterol: every company that makes it
- Form
- solution, respiratory (inhalation)
- Strength
- 1.25 mg per 3 mL
- Approval
- ANDA ANDA215571
- On the market since
- Nov 1, 2024
- Package NDCs
50742-393-0550742-393-25- Official label
- DailyMed (National Library of Medicine), updated Oct 22, 2024
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