Hydroxyzine Hydrochloride

Product NDC

63629-6518

11-digit product format

636296518

Labeler code

63629

Product ID

63629-6518_917af184-cb06-4edc-aa2a-6099512e7549

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

hydroxyzine hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA091176

Marketing category

ANDA

Marketing start

2010-07-23

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