Bupropion Hydrochloride

Product NDC

70518-0788

11-digit product format

705180788

Labeler code

70518

Product ID

70518-0788_67d8ad4b-fb46-a3d3-e053-2991aa0af8c3

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

bupropion hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA075491

Marketing category

ANDA

Marketing start

2017-10-17

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