Bupropion Hydrochloride

Product NDC

50090-3139

11-digit product format

500903139

Labeler code

50090

Product ID

50090-3139_44302baf-7c4f-4639-808d-395e13667b52

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Bupropion Hydrochloride

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA077715

Marketing category

ANDA

Marketing start

2008-11-26

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

2019-12-31

Current FDA listing

Historical FDA.report record