NDC 0591-3543
Bupropion HydrochlorideSR 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.
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 150 mg
- Approval
- ANDA ANDA079094
- On the market since
- Jun 11, 2009
- Package NDCs
0591-3543-600591-3543-76- Official label
- DailyMed (National Library of Medicine), updated Sep 30, 2025
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