NDC 71205-387
Bupropion Hydrochloride 100 mg tablet, extended release
On the label: Proficient Rx LP. It's repackaged from NDC 0185-0410, 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 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 Proficient Rx LP names for other drugs.
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, extended release
- Strength
- 100 mg
- Approval
- ANDA ANDA075932
- On the market since
- Nov 25, 2003
- Package NDCs
71205-387-3071205-387-6071205-387-90- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2020
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?