NDC 71209-052
Bupropion Hydrochloride 75 mg tablet, film coated
On the label: Cadila Pharmaceuticals Limited.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Cadila Pharmaceuticals Limited | Ahmedabad, India | Makes it, tests it, packages it and labels it | No problems foundSep 26, 2025 · 7 inspections |
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 75 mg
- Approval
- ANDA ANDA208606
- On the market since
- Jan 16, 2020
- Package NDCs
71209-052-0571209-052-1171209-052-17- Official label
- DailyMed (National Library of Medicine), updated Mar 19, 2026
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