Bupropion hydrochloride

Product NDC

13668-432

11-digit product format

136680432

Labeler code

13668

Product ID

13668-432_64072372-9900-47b2-a46a-ba216a06cad3

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Bupropion hydrochloride

Dosage form

TABLET, EXTENDED RELEASE

Route

ORAL

Labeler

Torrent Pharmaceuticals Limited

Application

ANDA203969

Marketing category

ANDA

Marketing start

2014-10-31

Marketing end

0000-00-00

Substance

BUPROPION HYDROCHLORIDE

Active strength

200 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

2019-12-31

Current FDA listing

Historical FDA.report record