NDC 70518-4591
bupropion hydrochlorideSR 100 mg tablet, film coated, extended release
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Solco Healthcare U.S., LLC's NDC 43547-288.
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 Solco Healthcare U.S., LLC names for other drugs.
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 100 mg
- Approval
- ANDA ANDA202304
- On the market since
- Mar 20, 2026
- Package NDCs
70518-4591-0- Official label
- DailyMed (National Library of Medicine), updated Sep 17, 2026
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