NDC 66336-897
Bupropion Hydrochloride 150 mg tablet
On the label: Dispensing Solutions 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 Dispensing Solutions Inc. names for other drugs.
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet
- Strength
- 150 mg
- Approval
- ANDA ANDA077455
- On the market since
- Mar 12, 2008
- Package NDCs
66336-897-3066336-897-60- Official label
- DailyMed (National Library of Medicine), updated Sep 13, 2011
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