NDC 76282-642
BudesonideInhalation Suspension 1 mg per 2 mL inhalant
On the label: Exelan Pharmaceuticals, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Cipla Limited | Salcette, India | Makes it | Problems found, fixed voluntarilyJun 21, 2024 · 12 inspections, 2 with FDA action |
| Cipla Limited | Indore, India | Makes it | Serious problems, FDA actionFeb 17, 2023 · 6 inspections, 1 with FDA action |
Product details
- Generic drug
- Budesonide: every company that makes it
- Form
- inhalant, oral
- Strength
- 1 mg per 2 mL
- Approval
- ANDA ANDA205710
- On the market since
- Apr 19, 2019
- Package NDCs
76282-642-3776282-642-38- Official label
- DailyMed (National Library of Medicine), updated Dec 11, 2020
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