NDC 76420-812-01
Bupropion Hydrochloride 300 mg/1
Bupropion Hydrochloride · TABLET, EXTENDED RELEASE
Bupropion Hydrochloride is a tablet, extended release containing bupropion hydrochloride at a strength of 300 mg/1. Manufactured by Asclemed USA, Inc..
Key Facts
- Brand Name
- Bupropion Hydrochloride
- Generic Name
- Bupropion Hydrochloride
- NDC Code (Package)
76420-812-01- NDC Code (Product)
76420-812- Manufacturer
- Asclemed USA, Inc.
- Strength
- 300 mg/1
- Dosage Form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- ANDA077285
- Marketing Start
- 02/17/2015
Recall History
No Recall HistoryView Full Drug Page
Bupropion Hydrochloride — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.