NDC 43598-538
Bupropion Hydrochloride SR 200 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 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
- 200 mg
- Approval
- ANDA ANDA205794
- On the market since
- Aug 1, 2016
- Package NDCs
43598-538-60- Official label
- DailyMed (National Library of Medicine), updated Dec 23, 2022
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