Hydroxyzine Hydrochloride

Product NDC

50090-0122

11-digit product format

500900122

Labeler code

50090

Product ID

50090-0122_c15ea798-8d97-40a5-96c7-f41790d91048

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

hydroxyzine hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA040786

Marketing category

ANDA

Marketing start

2012-07-24

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