NDC 55648-102
Bupropion Hydrochloride(XL) 150 mg tablet, film coated, extended release
On the label: Wockhardt Limited.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Wockhardt Limited | Location not on file | Makes it, tests it, packages it and labels it | Not inspected on record |
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, film coated, extended release
- Strength
- 150 mg
- Approval
- ANDA ANDA202189
- On the market since
- Nov 21, 2012
- Package NDCs
55648-102-0155648-102-02- Official label
- DailyMed (National Library of Medicine), updated Apr 10, 2015
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