Bupropion Hydrochloride

Product NDC

59746-315

11-digit product format

597460315

Labeler code

59746

Product ID

59746-315_8156434c-b751-473e-906d-36c175c63797

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

bupropion hydrochloride

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

Jubilant Cadista Pharmaceuticals Inc.

Application

ANDA202774

Marketing category

ANDA

Marketing start

2013-10-11

Marketing end

0000-00-00

Substance

BUPROPION HYDROCHLORIDE

Active strength

100 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