NDC 43598-656
Bupropion Hydrochloride (XL) 300 mg tablet, film coated, extended release
On the label: Dr. Reddy's Laboratories Inc..
Where it's 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
- 300 mg
- Approval
- ANDA ANDA207479
- On the market since
- Apr 12, 2017
- Package NDCs
43598-656-0543598-656-3043598-656-90- Official label
- DailyMed (National Library of Medicine), updated Sep 16, 2026
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