NDC 80425-0468
Bupropion HydrochlorideXL 300 mg tablet, extended release
On the label: Advanced Rx Pharmacy of Tennessee, LLC. It's repackaged from NDC 69367-289, made by Westminster Pharmaceuticals, LLC (Bupropion Hydrochloride). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were made
This label doesn't name the factory that makes the drug (it lists 1 site that repackages it). 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 Advanced Rx Pharmacy of Tennessee, LLC names for other drugs.
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 300 mg
- Approval
- ANDA ANDA207224
- On the market since
- Jan 1, 2025
- Package NDCs
80425-0468-180425-0468-280425-0468-3- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2025
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