BuPROPion Hydrochloride

Product NDC

0615-6553

11-digit product format

006156553

Labeler code

0615

Product ID

0615-6553_6368546a-d551-4e72-8949-8647e8416903

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

BuPROPion Hydrochloride

Dosage form

TABLET, EXTENDED RELEASE

Route

ORAL

Labeler

NCS HealthCare of KY, Inc dba Vangard Labs

Application

ANDA079095

Marketing category

ANDA

Marketing start

2009-07-02

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

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record