NDC 67046-082
Bupropion Hydrochloride 150 mg tablet, film coated, extended release
On the label: Coupler Enterprises Inc.. It's repackaged from NDC 10370-101, made by Par Pharmaceutical, 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 Coupler Enterprises 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 ANDA077284
- On the market since
- Sep 28, 2017
- Package NDCs
67046-082-0767046-082-1467046-082-1567046-082-2067046-082-2167046-082-2867046-082-3067046-082-60- Official label
- DailyMed (National Library of Medicine), updated Sep 28, 2017
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?