NDC 70934-704
bupropion Hydrochloride 100 mg tablet
On the label: Denton Pharma, Inc. DBA Northwind Pharmaceuticals.. It's repackaged: Denton Pharma, Inc. DBA Northwind Pharmaceuticals. rebottles it from Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.'s NDC 23155-192.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Heritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Labs Inc. | East Brunswick, NJ, United States | Makes it, tests it, packages it and labels it | No problems foundSep 19, 2023 · 10 inspections |
Repackaging site
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals, Location not on file · repackages it
Recalls
- Mar 15, 2021 · Class II · Cardinal Health Inc.
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Lots: L200791
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet
- Strength
- 100 mg
- Approval
- ANDA ANDA206975
- On the market since
- May 13, 2020
- Package NDCs
70934-704-6070934-704-90- Official label
- DailyMed (National Library of Medicine), updated Jul 13, 2020
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