NDC 0591-3331
Bupropion HydrochlorideXL 150 mg tablet, film coated, extended release
On the label: Actavis Pharma, Inc..
Where it's 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 Actavis Pharma, Inc. names for other drugs.
Recalls
- Nov 15, 2013 · Class III · Actavis Inc
Failed Dissolution Specifications: Failed stability testing for dissolution test at 18 months.
Lots: Lots: 524099M, 524100A, 521687A
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 150 mg
- Approval
- ANDA ANDA077715
- On the market since
- Nov 26, 2008
- Package NDCs
0591-3331-050591-3331-190591-3331-30- Official label
- DailyMed (National Library of Medicine), updated Jul 16, 2026
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