Bupropion Hydrochloride

Product NDC

51079-109

11-digit product format

510790109

Labeler code

51079

Product ID

51079-109_7b1ff970-5ff5-738c-e053-2a91aa0ab2de

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

bupropion hydrochloride

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

Mylan Institutional Inc.

Application

ANDA090942

Marketing category

ANDA

Marketing start

2011-07-18

Marketing end

0000-00-00

Substance

BUPROPION HYDROCHLORIDE

Active strength

300 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