NDC 47335-954-13
Bupropion Hydrochloride 150 mg/1
Bupropion Hydrochloride · TABLET, EXTENDED RELEASE
Bupropion Hydrochloride is a tablet, extended release containing bupropion hydrochloride at a strength of 150 mg/1. Manufactured by Sun Pharmaceutical Industries, Inc..
Key Facts
- Brand Name
- Bupropion Hydrochloride
- Generic Name
- Bupropion Hydrochloride
- NDC Code (Package)
47335-954-13- NDC Code (Product)
47335-954- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Strength
- 150 mg/1
- Dosage Form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- ANDA200695
- Marketing Start
- 12/25/2014
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.