NDC 70518-3963
Bupropion Hydrochloride(XL) 150 mg tablet, film coated, extended release
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from ScieGen Pharmaceuticals, Inc.'s NDC 50228-144.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| ScieGen Pharmaceuticals, INC. | Hauppauge, NY, United States | Makes it, tests it and labels it | Problems found, fixed voluntarilyMay 15, 2026 · 15 inspections, 1 with FDA action |
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 150 mg
- Approval
- ANDA ANDA207479
- On the market since
- Dec 14, 2023
- Package NDCs
70518-3963-070518-3963-170518-3963-270518-3963-370518-3963-4- Official label
- DailyMed (National Library of Medicine), updated Aug 20, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?