Bupropion Hydrochloride

Product NDC

63739-714

11-digit product format

637390714

Labeler code

63739

Product ID

63739-714_f5086bf9-4f34-4dcd-b450-cf1aba166987

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Bupropion Hydrochloride

Dosage form

TABLET, EXTENDED RELEASE

Route

ORAL

Labeler

McKesson Corporation dba SKY Packaging

Application

ANDA075932

Marketing category

ANDA

Marketing start

2004-03-22

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