NDC 70518-4014-1
Bupropion Hydrochloride XL 300 mg/1
bupropion hydrochloride · TABLET, EXTENDED RELEASE
Bupropion Hydrochloride XL is a tablet, extended release containing bupropion hydrochloride at a strength of 300 mg/1. Manufactured by REMEDYREPACK INC..
Key Facts
- Brand Name
- Bupropion Hydrochloride XL
- Generic Name
- bupropion hydrochloride
- NDC Code (Package)
70518-4014-1- NDC Code (Product)
70518-4014- Manufacturer
- REMEDYREPACK INC.
- Strength
- 300 mg/1
- Dosage Form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- ANDA210015
- Marketing Start
- 02/07/2024
Recall History
No Recall HistoryView Full Drug Page
Bupropion Hydrochloride XL — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.