NDC 76420-812
Bupropion Hydrochloride 300 mg tablet, extended release
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Actavis Pharma, Inc.'s NDC 45963-142.
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 Actavis Pharma, Inc. names for other drugs.
Repackaging site
- Asclemed USA Inc. dba Enovachem, Torrance, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 300 mg
- Approval
- ANDA ANDA077285
- On the market since
- Feb 17, 2015
- Package NDCs
76420-812-0176420-812-0576420-812-3076420-812-6076420-812-90- Official label
- DailyMed (National Library of Medicine), updated Feb 12, 2025
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