ZYBAN

Product NDC

0173-0556

11-digit product format

001730556

Labeler code

0173

Product ID

0173-0556_72435712-b707-4d63-a9a4-697a3bfa2bc6

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

bupropion hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

GlaxoSmithKline LLC

Application

NDA020711

Marketing category

NDA

Marketing start

1997-05-28

Marketing end

0000-00-00

Substance

BUPROPION HYDROCHLORIDE

Active strength

150 mg/1

Pharmacologic classes

Aminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [MoA]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record