NDC 43353-735
Bupropion Hydrochloride 100 mg tablet, film coated, extended release
On the label: Aphena Pharma Solutions - Tennessee, Inc.. It's repackaged from NDC 67767-171, made by Actavis South Atlantic 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 Aphena Pharma Solutions - Tennessee, Inc. names for other drugs.
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, film coated, extended release
- Strength
- 100 mg
- Approval
- ANDA ANDA077455
- On the market since
- Jul 19, 2010
- Package NDCs
43353-735-82- Official label
- DailyMed (National Library of Medicine), updated Aug 16, 2012
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?