Bupropion hydrochloride

Product NDC

71335-0783

11-digit product format

713350783

Labeler code

71335

Product ID

71335-0783_2c96ab0d-93b4-4592-ad6b-592555377621

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Bupropion hydrochloride

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA090325

Marketing category

ANDA

Marketing start

2010-04-09

Marketing end

0000-00-00

Substance

BUPROPION HYDROCHLORIDE

Active strength

100 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

2019-12-31

Current FDA listing

Historical FDA.report record