NDC 59651-511
Bupropion Hydrochloride 150 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
- 150 mg
- Approval
- ANDA ANDA216051
- On the market since
- Jul 21, 2026
- Package NDCs
59651-511-0559651-511-3059651-511-90- Official label
- DailyMed (National Library of Medicine), updated Jul 23, 2026
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