NDC 33261-627
Bupropion Hydrochloride 300 mg tablet, film coated, extended release
On the label: Aidarex Pharmaceuticals LLC. It's repackaged from NDC 10370-102, made by Par Pharmaceutical, 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. 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 Aidarex Pharmaceuticals LLC names for other drugs.
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, film coated, extended release
- Strength
- 300 mg
- Approval
- ANDA ANDA077284
- On the market since
- Jun 12, 2007
- Package NDCs
33261-627-30- Official label
- DailyMed (National Library of Medicine), updated Dec 14, 2013
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