NDC 16590-038
Bupropion Hydrochloride 150 mg tablet, film coated, extended release
On the label: Stat Rx USA. It's repackaged: Stat Rx USA rebottles it from Actavis Pharma, Inc.'s NDC 0591-3541.
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 Actavis Pharma, Inc. names for other drugs.
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, film coated, extended release
- Strength
- 150 mg
- Approval
- ANDA ANDA079095
- On the market since
- Jul 2, 2009
- Package NDCs
16590-038-3016590-038-5616590-038-6016590-038-90- Official label
- DailyMed (National Library of Medicine), updated Aug 26, 2010
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?