NDC 42708-205
bupropion hydrochlorideSR 150 mg tablet, film coated, extended release
On the label: QPharma, Inc.. It's repackaged: QPharma, Inc. rebottles it from Solco Healthcare U.S., LLC's NDC 43547-289.
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 Solco Healthcare U.S., LLC names for other drugs.
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 150 mg
- Approval
- ANDA ANDA202304
- On the market since
- Nov 1, 2014
- Package NDCs
42708-205-60- Official label
- DailyMed (National Library of Medicine), updated Oct 15, 2026
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