Bupropion Hydrochloride

Product NDC

0378-5521

11-digit product format

003785521

Labeler code

0378

Product ID

0378-5521_b409d8aa-b3a3-4ff8-9d9b-89db580120bf

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Bupropion Hydrochloride

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

Mylan Pharmaceuticals Inc.

Application

ANDA090941

Marketing category

ANDA

Marketing start

2010-05-14

Marketing end

2019-11-30

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

0000-00-00

Current FDA listing

Historical FDA.report record