Cetirizine hydrochloride

Product NDC

68788-9985

11-digit product format

687889985

Labeler code

68788

Product ID

68788-9985_ac7af2b7-b851-4a87-abc7-7c296005a765

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Cetirizine hydrochloride

Dosage form

SOLUTION

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA078870

Marketing category

ANDA

Marketing start

2015-04-20

Marketing end

0000-00-00

Substance

CETIRIZINE HYDROCHLORIDE

Active strength

1 mg/mL

Pharmacologic classes

Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record