NDC 70934-791
Bupropion HydrochlorideSR 150 mg tablet, film coated, extended release
On the label: Denton Pharma, Inc. DBA Northwind Pharmaceuticals.. It's repackaged: Denton Pharma, Inc. DBA 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
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals, Location not on file · repackages it
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, film coated, extended release
- Strength
- 150 mg
- Approval
- ANDA ANDA205794
- On the market since
- Sep 8, 2020
- Package NDCs
70934-791-3070934-791-6070934-791-9070934-791-96- Official label
- DailyMed (National Library of Medicine), updated Apr 29, 2021
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