NDC 60687-889
Budesonide 0.25 mg per 2 mL suspension
On the label: American Health Packaging. It's repackaged: American Health Packaging rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 47335-631.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Sun Pharmaceutical Industries Limited (formerly known as Sun Pharmaceutical Medicare Limited) | Halol Panchmahal, India | Makes it and tests it | No problems foundFeb 27, 2024 · 4 inspections |
Repackaging site
- American Health Packaging, Columbus, OH, United States · repackages it
Recalls
- May 29, 2026 · Class II · Sun Pharmaceutical Industries Inc
Presence of Foreign Substance:This recall has been initiated in response to a product quality complaint reported for black/brown specs and particles within the ampoule solution
Lots: Lot #: BAG0074A, Exp. Date: 1/31/2027.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Budesonide: every company that makes it
- Form
- suspension, respiratory (inhalation)
- Strength
- 0.25 mg per 2 mL
- Approval
- ANDA ANDA211922
- On the market since
- May 15, 2026
- Package NDCs
60687-889-7960687-889-83- Official label
- DailyMed (National Library of Medicine), updated May 18, 2026
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