NDC 71335-0824
Bupropion hydrochloride (XL) 300 mg tablet, extended release
On the label: Bryant Ranch Prepack. It's repackaged from NDC 0781-5529, 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 and relabels 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 Bryant Ranch Prepack names for other drugs.
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, extended release
- Strength
- 300 mg
- Approval
- ANDA ANDA208652
- On the market since
- Jan 8, 2018
- Package NDCs
71335-0824-171335-0824-271335-0824-371335-0824-471335-0824-5- Official label
- DailyMed (National Library of Medicine), updated Sep 17, 2020
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