NDC 71205-394
Bupropion HydrochlorideXL 150 mg tablet, extended release
On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from Slate Run Pharmaceuticals, LLC.'s NDC 70436-010.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Yichang Humanwell Oral Solid Dosage Plant | Yichang, China | Makes it | No problems foundJul 21, 2023 · 2 inspections |
Repackaging site
- Proficient Rx LP, Thousand Oaks, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 150 mg
- Approval
- ANDA ANDA210015
- On the market since
- Dec 1, 2018
- Package NDCs
71205-394-3071205-394-6071205-394-90- Official label
- DailyMed (National Library of Medicine), updated Feb 1, 2020
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