NDC 67046-1648
Bupropion hydrochloride 300 mg tablet, extended release
On the label: Coupler LLC. It's repackaged: Coupler LLC rebottles it from Granules Pharmaceuticals Inc.'s NDC 70010-785.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Granules Pharmaceuticals Inc. names for other drugs.
Repackaging site
- Coupler LLC, West Chester, PA, United States · repackages it
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 300 mg
- Approval
- ANDA ANDA215568
- On the market since
- Jan 15, 2026
- Package NDCs
67046-1648-3- Official label
- DailyMed (National Library of Medicine), updated Jan 15, 2026
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