NDC 64980-644
Albuterol Sulfate 1.25 mg per 3 mL solution
On the label: Rising Pharma Holdings, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Nephron SC, LLC | West Columbia, SC, United States | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyAug 22, 2025 · 26 inspections, 10 with FDA action |
Product details
- Generic drug
- Albuterol: every company that makes it
- Form
- solution, respiratory (inhalation)
- Strength
- 1.25 mg per 3 mL
- Approval
- ANDA ANDA076355
- On the market since
- Apr 14, 2025
- Package NDCs
64980-644-02- Official label
- DailyMed (National Library of Medicine), updated Jul 16, 2026
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