NDC 61919-136
Bupropion Hydrochloride 150 mg tablet, extended release
On the label: Direct Rx. It's repackaged from NDC 0185-0415, made by Eon Labs, 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, extended release
- Strength
- 150 mg
- Approval
- ANDA ANDA075932
- On the market since
- Jul 17, 2017
- Package NDCs
61919-136-3061919-136-60- Official label
- DailyMed (National Library of Medicine), updated Apr 21, 2022
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?