NDC 70518-3560
Albuterol Sulfate 0.83 mg per 1 mL solution
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 47335-703.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Sun Pharmaceutical Industries Limited (formerly known as Sun Pharmaceutical Medicare Limited) | Halol Panchmahal, India | Makes it and tests it | No problems foundFeb 27, 2024 · 4 inspections |
Product details
- Generic drug
- Albuterol: every company that makes it
- Form
- solution, respiratory (inhalation)
- Strength
- 0.83 mg per 1 mL
- Approval
- ANDA ANDA207857
- On the market since
- Oct 19, 2022
- Package NDCs
70518-3560-070518-3560-1- Official label
- DailyMed (National Library of Medicine), updated Jun 17, 2026
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