Drugplain

NDC 63187-052-60

Bupropion hydrochloride 150 mg/1

Bupropion hydrochloride · TABLET, FILM COATED, EXTENDED RELEASE

No Recall History

Bupropion hydrochloride is a tablet, film coated, extended release containing bupropion hydrochloride at a strength of 150 mg/1. Manufactured by Proficient Rx LP.

Key Facts

Brand Name
Bupropion hydrochloride
Generic Name
Bupropion hydrochloride
NDC Code (Package)
63187-052-60
NDC Code (Product)
63187-052
Manufacturer
Proficient Rx LP
Strength
150 mg/1
Dosage Form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Marketing Status
Application #
ANDA078866
Marketing Start
04/08/2010

Recall History

No Recall History

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