NDC 72516-035
buPropion Hydrochloride XL 150 mg tablet, extended release
On the label: Oryza Pharmaceuticals Inc..
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 Oryza Pharmaceuticals Inc. names for other drugs.
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 150 mg
- Approval
- ANDA ANDA211200
- On the market since
- Oct 1, 2020
- Package NDCs
72516-035-0372516-035-0972516-035-50- Official label
- DailyMed (National Library of Medicine), updated Nov 25, 2025
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