NDC 47335-736-13
Bupropion hydrochloride 100 mg/1
Bupropion hydrochloride · TABLET, FILM COATED, EXTENDED RELEASE
Bupropion hydrochloride is a tablet, film coated, extended release containing bupropion hydrochloride at a strength of 100 mg/1. Manufactured by Sun Pharmaceutical Industries, Inc..
Key Facts
- Brand Name
- Bupropion hydrochloride
- Generic Name
- Bupropion hydrochloride
- NDC Code (Package)
47335-736-13- NDC Code (Product)
47335-736- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Strength
- 100 mg/1
- Dosage Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- ANDA078866
- Marketing Start
- 03/01/2020
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.