NDC 10370-204
Bupropion Hydrochloride 150 mg tablet, film coated, extended release
On the label: Par Pharmaceutical 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 Par Pharmaceutical Inc. names for other drugs.
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, film coated, extended release
- Strength
- 150 mg
- Approval
- ANDA ANDA091520
- On the market since
- Jan 1, 2026
- Package NDCs
10370-204-0010370-204-06- Official label
- DailyMed (National Library of Medicine), updated Oct 30, 2017
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?