NDC 0115-6811
Bupropion Hydrochloride 150 mg tablet, film coated, extended release
On the label: Amneal Pharmaceuticals.
Where it's made
This label doesn't name the factory that makes the drug (it lists 1 site that packages 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 Amneal Pharmaceuticals names for other drugs.
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 150 mg
- Approval
- ANDA ANDA077415
- On the market since
- May 1, 2009
- Package NDCs
0115-6811-020115-6811-080115-6811-10- Official label
- DailyMed (National Library of Medicine), updated Mar 27, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?