NDC 59651-848
Bupropion Hydrochloride 200 mg tablet, film coated, extended release
On the label: Aurobindo Pharma Limited.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Apl Healthcare Limited | Tirupati, India | Makes it and tests it | Problems found, fixed voluntarilyDec 17, 2025 · 5 inspections |
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 200 mg
- Approval
- ANDA ANDA090325
- On the market since
- Jun 3, 2025
- Package NDCs
59651-848-0159651-848-60- Official label
- DailyMed (National Library of Medicine), updated Nov 14, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?