NDC 70010-127
Bupropion Hydrochloride 200 mg tablet, film coated, extended release
On the label: Granules Pharmaceuticals Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Granules Pharmaceuticals Inc. | Chantilly, VA, United States | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyApr 3, 2026 · 6 inspections |
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 200 mg
- Approval
- ANDA ANDA218385
- On the market since
- Mar 31, 2025
- Package NDCs
70010-127-0370010-127-0570010-127-06- Official label
- DailyMed (National Library of Medicine), updated Oct 8, 2026
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