NDC 16571-863-03
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 Rising Pharma Holdings, Inc..
Key Facts
- Brand Name
- bupropion hydrochloride
- Generic Name
- bupropion hydrochloride
- NDC Code (Package)
16571-863-03- NDC Code (Product)
16571-863- Manufacturer
- Rising Pharma Holdings, Inc.
- Strength
- 300 mg/1
- Dosage Form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- ANDA211020
- Marketing Start
- 08/01/2022
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.