NDC 0440-7200
Bupropion Hydrochloride 150 mg tablet, film coated, extended release
On the label: Liberty Pharmaceuticals, Inc.. It's repackaged from NDC 67767-133, made by Actavis South Atlantic LLC (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 Liberty Pharmaceuticals, Inc. names for other drugs.
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, film coated, extended release
- Strength
- 150 mg
- Approval
- ANDA ANDA077455
- On the market since
- Mar 12, 2008
- Package NDCs
0440-7200-300440-7200-600440-7200-810440-7200-900440-7200-910440-7200-92- Official label
- DailyMed (National Library of Medicine), updated Aug 10, 2016
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