NDC 0115-5445
Bupropion Hydrochloride 200 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. 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
- 200 mg
- Approval
- ANDA ANDA076711
- On the market since
- Dec 3, 2004
- Package NDCs
0115-5445-13- Official label
- DailyMed (National Library of Medicine), updated May 9, 2024
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