NDC 21695-578
Bupropion HydrochlorideXL 300 mg tablet, film coated, extended release
On the label: Rebel Distributors Corp... It's repackaged from NDC 0591-3332, made by Actavis Pharma, 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 Rebel Distributors Corp.. 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 ANDA077715
- On the market since
- Jun 13, 2007
- Package NDCs
21695-578-30- Official label
- DailyMed (National Library of Medicine), updated Sep 17, 2010
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