NDC 68258-7157
Bupropion hydrochloride 100 mg tablet, film coated, extended release
On the label: Dispensing Solutions Inc.. It's repackaged from NDC 47335-736, made by Sun Pharmaceutical Industries, 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 Dispensing Solutions Inc. names for other drugs.
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, film coated, extended release
- Strength
- 100 mg
- Approval
- ANDA ANDA078866
- On the market since
- Apr 8, 2010
- Package NDCs
68258-7157-368258-7157-668258-7157-9- Official label
- DailyMed (National Library of Medicine), updated Oct 31, 2013
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