NDC 68258-8922
Budesonide 0.5 mg per 2 mL suspension
On the label: Dispensing Solutions Inc.. It's repackaged: Dispensing Solutions Inc. rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 0093-6816.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Teva Pharmaceuticals USA, Inc. names for other drugs.
Repackaging site
- Dispensing Solutions Inc., Santa Ana, California, United States · repackages it and relabels it
Product details
- Generic drug
- Budesonide: every company that makes it
- Form
- suspension
- Strength
- 0.5 mg per 2 mL
- Approval
- ANDA ANDA077519
- On the market since
- Nov 19, 2008
- Package NDCs
68258-8922-5- Official label
- DailyMed (National Library of Medicine), updated Aug 30, 2013
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