Bupropion Hydrochloride

Product NDC

68071-2192

11-digit product format

680712192

Labeler code

68071

Product ID

68071-2192_4bcdf2c6-dc1e-558f-e054-00144ff8d46c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

bupropion hydrochloride

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

ANDA079095

Marketing category

ANDA

Marketing start

2009-07-02

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

2019-12-31

Current FDA listing

Historical FDA.report record