Bupropion Hydrochloride

Product NDC

50090-2721

11-digit product format

500902721

Labeler code

50090

Product ID

50090-2721_9d7111f6-9a52-4189-9c3c-8e08016dd75f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Bupropion Hydrochloride

Dosage form

TABLET, EXTENDED RELEASE

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA077285

Marketing category

ANDA

Marketing start

2015-02-17

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