NDC 76204-018
Budesonide Inhalation Suspension 0.5 mg per 2 mL suspension
On the label: Ritedose Pharmaceuticals, LLC. It's repackaged: Ritedose Pharmaceuticals, LLC rebottles it from Lupin Pharmaceuticals, Inc.'s NDC 68180-984.
Where the pills inside were 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 |
Repackaging site
- The Ritedose Corporation, Columbia, SC, United States · makes it, tests it, packages it, labels it and repackages it
Product details
- Generic drug
- Budesonide: every company that makes it
- Form
- suspension
- Strength
- 0.5 mg per 2 mL
- Approval
- ANDA ANDA210897
- On the market since
- Dec 1, 2021
- Package NDCs
76204-018-0176204-018-11- Official label
- DailyMed (National Library of Medicine), updated Dec 16, 2022
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?