NDC 70518-4613
budesonide 3 mg capsule, coated pellets
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Northstar Rx LLC.'s NDC 16714-829.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zydus Lifesciences Limited | Ahmedabad, India | Makes it and tests it | Problems found, fixed voluntarilyMar 24, 2023 · 5 inspections |
Product details
- Generic drug
- Budesonide: every company that makes it
- Form
- capsule, coated pellets, oral
- Strength
- 3 mg
- Approval
- ANDA ANDA206134
- On the market since
- Apr 23, 2026
- Package NDCs
70518-4613-070518-4613-1- Official label
- DailyMed (National Library of Medicine), updated May 21, 2026
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