hydroxyzine hydrochloride

Product NDC

50090-2650

11-digit product format

500902650

Labeler code

50090

Product ID

50090-2650_e9d37118-2342-497c-adf9-4452ad4ca23c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

hydroxyzine hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA040812

Marketing category

ANDA

Marketing start

2015-02-01

Marketing end

0000-00-00

Substance

HYDROXYZINE HYDROCHLORIDE

Active strength

25 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