NDC 61919-037
Bupropion Hydrochloride 75 mg tablet, film coated
On the label: Direct Rx. It's repackaged from NDC 0781-1053, 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). 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 Direct Rx names for other drugs.
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, film coated
- Strength
- 75 mg
- Approval
- ANDA ANDA075584
- On the market since
- Nov 25, 2015
- Package NDCs
61919-037-3061919-037-60- Official label
- DailyMed (National Library of Medicine), updated Oct 15, 2019
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?