Hydroxyzine Hydrochloride

Product NDC

70518-2159

11-digit product format

705182159

Labeler code

70518

Product ID

70518-2159_9734bfae-2b57-2d81-e053-2995a90a21fe

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Hydroxyzine Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA088619

Marketing category

ANDA

Marketing start

2019-06-27

Marketing end

0000-00-00

Substance

HYDROXYZINE HYDROCHLORIDE

Active strength

50 mg/1

Pharmacologic classes

Antihistamine [EPC],Histamine Receptor Antagonists [MoA]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record