NDC 70934-724
Bupropion hydrochloride (XL) 150 mg tablet, extended release
On the label: Denton Pharma, Inc. DBA Northwind Pharmaceuticals.. It's repackaged from NDC 0781-5528, made by Sandoz Inc. (Bupropion hydrochloride (XL)). 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 (it lists 1 site that repackages it). 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 Denton Pharma, Inc. DBA Northwind Pharmaceuticals. names for other drugs.
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, extended release
- Strength
- 150 mg
- Approval
- ANDA ANDA208652
- On the market since
- May 20, 2020
- Package NDCs
70934-724-3070934-724-90- Official label
- DailyMed (National Library of Medicine), updated Jul 9, 2020
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