NDC 50436-9101
Bupropion Hydrochloride 100 mg tablet, film coated
On the label: Unit Dose Services. It's repackaged from NDC 0781-1064, made by Sandoz 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 and relabels 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 Unit Dose Services names for other drugs.
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, film coated
- Strength
- 100 mg
- Approval
- ANDA ANDA075584
- On the market since
- Feb 7, 2000
- Package NDCs
50436-9101-2- Official label
- DailyMed (National Library of Medicine), updated Jul 1, 2017
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?