NDC 82868-019
Bupropion HydrochlorideSR 150 mg tablet, film coated, extended release
On the label: Northwind Pharmaceuticals. It's repackaged: Northwind Pharmaceuticals rebottles it from ScieGen Pharmaceuticals, Inc.'s NDC 50228-175.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| ScieGen Pharmaceuticals, INC. | Hauppauge, NY, United States | Makes it and tests it | Problems found, fixed voluntarilyMay 15, 2026 · 15 inspections, 1 with FDA action |
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 150 mg
- Approval
- ANDA ANDA205794
- On the market since
- Oct 19, 2023
- Package NDCs
82868-019-3082868-019-6082868-019-9082868-019-96- Official label
- DailyMed (National Library of Medicine), updated Jun 19, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?