NDC 47335-954
Bupropion Hydrochloride 150 mg tablet, extended release
On the label: Caraco Pharmaceutical Laboratories, Ltd..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Sun Pharmaceutical Industries Limited | Dadra, India | Makes it and tests it | Problems found, fixed voluntarilyMar 29, 2019 · 5 inspections |
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 150 mg
- Approval
- ANDA ANDA200695
- On the market since
- Dec 25, 2014
- Package NDCs
47335-954-1347335-954-8147335-954-83- Official label
- DailyMed (National Library of Medicine), updated Oct 31, 2018
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