Bupropion Hydrochloride

Product NDC

50090-0785

11-digit product format

500900785

Labeler code

50090

Product ID

50090-0785_d67c4dfc-6b05-4eb7-a740-2b76b8899973

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Bupropion Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA075584

Marketing category

ANDA

Marketing start

2000-02-07

Marketing end

0000-00-00

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

2019-12-31

Current FDA listing

Historical FDA.report record