Hydroxyzine Hydrochloride

Product NDC

42708-060

11-digit product format

427080060

Labeler code

42708

Product ID

42708-060_0df59791-c99b-4b6a-820d-193f157a4a82

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Hydroxyzine Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

QPharma Inc

Application

ANDA040840

Marketing category

ANDA

Marketing start

2009-11-11

Marketing end

0000-00-00

Substance

HYDROXYZINE HYDROCHLORIDE

Active strength

10 mg/1

Pharmacologic classes

Antihistamine [EPC],Histamine Receptor Antagonists [MoA]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record