BUPROPION HYDROCHLORIDE

Product NDC

61919-921

11-digit product format

619190921

Labeler code

61919

Product ID

61919-921_85a4efa6-070f-e2f0-e053-2991aa0aaf01

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

BUPROPION HYDROCHLORIDE

Dosage form

TABLET, EXTENDED RELEASE

Route

ORAL

Labeler

DIRECT RX

Application

ANDA075932

Marketing category

ANDA

Marketing start

2018-03-14

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