Bupropion Hydrochloride

Product NDC

55700-684

11-digit product format

557000684

Labeler code

55700

Product ID

55700-684_1cdbfb6a-a017-4fc9-bebf-5c83037df9e5

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

BUPROPION HYDROCHLORIDE

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

ANDA077415

Marketing category

ANDA

Marketing start

2018-09-14

Marketing end

0000-00-00

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

2020-12-31

Current FDA listing

Historical FDA.report record