NDC 70518-4189
Bupropion hydrochloride 150 mg tablet, extended release
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Granules Pharmaceuticals Inc.'s NDC 70010-784.
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 Granules Pharmaceuticals Inc. names for other drugs.
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 150 mg
- Approval
- ANDA ANDA215568
- On the market since
- Sep 26, 2024
- Package NDCs
70518-4189-070518-4189-1- Official label
- DailyMed (National Library of Medicine), updated Jul 22, 2026
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