NDC 43353-189
Bupropion Hydrochloride 200 mg tablet, extended release
On the label: Aphena Pharma Solutions - Tennessee, Inc.. It's repackaged from NDC 0185-1111, made by Eon Labs, Inc. (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, extended release
- Strength
- 200 mg
- Approval
- ANDA ANDA075932
- On the market since
- Jun 22, 2005
- Package NDCs
43353-189-83- Official label
- DailyMed (National Library of Medicine), updated Dec 17, 2019
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?