Bupropion Hydrochloride

Product NDC

68001-199

11-digit product format

680010199

Labeler code

68001

Product ID

68001-199_92d86a41-70c0-4574-b052-6c7f5f23d246

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Bupropion Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

BluePoint Laboratories

Application

ANDA075584

Marketing category

ANDA

Marketing start

2014-02-07

Marketing end

2019-07-31

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

0000-00-00

Current FDA listing

Historical FDA.report record