Drugplain

NDC 68180-319-02

Bupropion Hydrochloride XL 150 mg/1

Bupropion Hydrochloride · TABLET, EXTENDED RELEASE

No Recall History

Bupropion Hydrochloride XL is a tablet, extended release containing bupropion hydrochloride at a strength of 150 mg/1. Manufactured by Lupin Pharmaceuticals, Inc..

Key Facts

Brand Name
Bupropion Hydrochloride XL
Generic Name
Bupropion Hydrochloride
NDC Code (Package)
68180-319-02
NDC Code (Product)
68180-319
Manufacturer
Lupin Pharmaceuticals, Inc.
Strength
150 mg/1
Dosage Form
TABLET, EXTENDED RELEASE
Route
ORAL
Marketing Status
Application #
ANDA090693
Marketing Start
06/14/2017

Recall History

No Recall History

Not medical advice. This information is for reference only. Always consult your doctor or pharmacist.