Bupropion Hydrochloride

Product NDC

51079-944

11-digit product format

510790944

Labeler code

51079

Product ID

51079-944_96261f61-2fe2-c957-e053-2a95a90a1545

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

bupropion hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Mylan Institutional Inc.

Application

ANDA075491

Marketing category

ANDA

Marketing start

2000-07-01

Marketing end

2020-09-30

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

0000-00-00

Current FDA listing

Historical FDA.report record