NDC 51655-357-26
bupropion 150 mg/1
bupropion hydrochloride · TABLET, FILM COATED, EXTENDED RELEASE
bupropion is a tablet, film coated, extended release containing bupropion hydrochloride at a strength of 150 mg/1. Manufactured by Northwind Health Company, LLC.
Key Facts
- Brand Name
- bupropion
- Generic Name
- bupropion hydrochloride
- NDC Code (Package)
51655-357-26- NDC Code (Product)
51655-357- Manufacturer
- Northwind Health Company, LLC
- Strength
- 150 mg/1
- Dosage Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- ANDA202304
- Marketing Start
- 05/28/2020
Recall History
No Recall HistoryView Full Drug Page
bupropion — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.