NDC 33358-364
Bupropion hydrochloride 150 mg tablet, film coated, extended release
On the label: RxChange Co.. It's repackaged from NDC 47335-736, made by Sun Pharmaceutical Industries, 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 RxChange Co. 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 ANDA078866
- On the market since
- Apr 8, 2010
- Package NDCs
33358-364-60- Official label
- DailyMed (National Library of Medicine), updated Dec 2, 2014
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?