NDC 0527-2415-32
Bupropion hydrochloride (XL) 150 mg/1
Bupropion hydrochloride · TABLET, EXTENDED RELEASE
Bupropion hydrochloride (XL) is a tablet, extended release containing bupropion hydrochloride at a strength of 150 mg/1. Manufactured by Lannett Company Inc..
Key Facts
- Brand Name
- Bupropion hydrochloride (XL)
- Generic Name
- Bupropion hydrochloride
- NDC Code (Package)
0527-2415-32- NDC Code (Product)
0527-2415- Manufacturer
- Lannett Company Inc.
- Strength
- 150 mg/1
- Dosage Form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- ANDA208652
- Marketing Start
- 01/08/2018
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.