NDC 0487-9601
Budesonide 0.25 mg per 2 mL inhalant
On the label: Nephron Pharmaceuticals Corporation.
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
- Budesonide: every company that makes it
- Form
- inhalant, respiratory (inhalation)
- Strength
- 0.25 mg per 2 mL
- Approval
- ANDA ANDA078202
- On the market since
- Oct 1, 2013
- Package NDCs
0487-9601-010487-9601-30- Official label
- DailyMed (National Library of Medicine), updated May 8, 2026
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