NDC 42254-185
BuPROPion Hydrochloride 100 mg tablet, film coated, extended release
On the label: Rebel Distributors Corp... It's repackaged: Rebel Distributors Corp.. rebottles it from Actavis Pharma, Inc.'s NDC 0591-3540.
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
- 100 mg
- Approval
- ANDA ANDA079095
- On the market since
- Jul 2, 2009
- Package NDCs
42254-185-60- Official label
- DailyMed (National Library of Medicine), updated Mar 20, 2012
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?