Bupropion Hydrochloride

Product NDC

49999-918

11-digit product format

499990918

Labeler code

49999

Product ID

49999-918_1c50448f-3189-4da8-b10e-b7c5e2a8ff25

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Bupropion Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

ANDA075584

Marketing category

ANDA

Marketing start

2000-02-07

Marketing end

0000-00-00

Substance

BUPROPION HYDROCHLORIDE

Active strength

75 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