NDC 53002-1508
Bupropion hydrochloride (XL) 300 mg tablet, extended release
On the label: RPK Pharmaceuticals, Inc.. 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 RPK Pharmaceuticals, Inc. 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
53002-1508-3- Official label
- DailyMed (National Library of Medicine), updated Dec 15, 2020
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?