NDC 77771-145
Bupropion Hydrochloride (XL) 300 mg tablet, film coated, extended release
On the label: Radha Pharmaceuticals, Inc..
Where it's 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 |
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 300 mg
- Approval
- ANDA ANDA207479
- On the market since
- Oct 26, 2022
- Package NDCs
77771-145-0577771-145-3077771-145-90- Official label
- DailyMed (National Library of Medicine), updated Feb 3, 2026
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