NDC 69097-071
Bupropion Hydrochloride 150 mg tablet, film coated, extended release
On the label: Cipla USA., Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| ScieGen Pharmaceuticals, INC. | Hauppauge, NY, United States | Makes it, tests it, packages 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
- 150 mg
- Approval
- ANDA ANDA207479
- On the market since
- Oct 25, 2023
- Package NDCs
69097-071-12- Official label
- DailyMed (National Library of Medicine), updated Oct 19, 2023
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