NDC 45865-885
Bupropion HydrochlorideSR 200 mg tablet, film coated, extended release
On the label: Medsource Pharmaceuticals. It's repackaged: Medsource Pharmaceuticals rebottles it from Actavis Pharma, Inc.'s NDC 0591-3542.
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.
Repackaging site
- Medsource Pharmaceuticals, Rancho Santa Margarita, CA, United States · repackages it
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, film coated, extended release
- Strength
- 200 mg
- Approval
- ANDA ANDA079095
- On the market since
- Jul 2, 2009
- Package NDCs
45865-885-30- Official label
- DailyMed (National Library of Medicine), updated Dec 24, 2018
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?