NDC 70518-3963-4
Bupropion Hydrochloride (XL) 150 mg/1
bupropion hydrochloride · TABLET, FILM COATED, EXTENDED RELEASE
Bupropion Hydrochloride (XL) is a tablet, film coated, extended release containing bupropion hydrochloride at a strength of 150 mg/1. Manufactured by REMEDYREPACK INC..
Key Facts
- Brand Name
- Bupropion Hydrochloride (XL)
- Generic Name
- bupropion hydrochloride
- NDC Code (Package)
70518-3963-4- NDC Code (Product)
70518-3963- Manufacturer
- REMEDYREPACK INC.
- Strength
- 150 mg/1
- Dosage Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- ANDA207479
- Marketing Start
- 12/14/2023
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.