Bupropion Hydrochloride

Product NDC

63739-706

11-digit product format

637390706

Labeler code

63739

Product ID

63739-706_1bf516a4-26f8-457e-8468-aa2b9f2a8694

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Bupropion Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

McKesson Corporation dba SKY Packaging

Application

ANDA075584

Marketing category

ANDA

Marketing start

2000-02-07

Marketing end

0000-00-00

Substance

BUPROPION HYDROCHLORIDE

Active strength

75 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