NDC 70518-1584
Bupropion Hydrochloride 100 mg tablet, film coated
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Apotex Corp.'s NDC 60505-0157.
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 Apotex Corp. names for other drugs.
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, film coated
- Strength
- 100 mg
- Approval
- ANDA ANDA076143
- On the market since
- Oct 24, 2018
- Package NDCs
70518-1584-070518-1584-1- Official label
- DailyMed (National Library of Medicine), updated Aug 21, 2025
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