Bupropion hydrochloride

Product NDC

13668-431

11-digit product format

136680431

Labeler code

13668

Product ID

13668-431_94801764-bab2-b762-e053-2995a90a5c3f

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

2021-07-31

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

0000-00-00

Current FDA listing

Historical FDA.report record