NDC 68180-984
budesonide inhalation 0.5 mg per 2 mL suspension
On the label: Lupin Pharmaceuticals, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| The Ritedose Corporation | Columbia, SC, United States | Makes it and packages it | Problems found, fixed voluntarilyFeb 28, 2025 · 12 inspections |
Product details
- Generic drug
- Budesonide: every company that makes it
- Form
- suspension, respiratory (inhalation)
- Strength
- 0.5 mg per 2 mL
- Approval
- ANDA ANDA210897
- On the market since
- May 21, 2019
- Package NDCs
68180-984-30- Official label
- DailyMed (National Library of Medicine), updated Jan 23, 2025
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