Levocetirizine Dihydrochloride

Product NDC

63629-4492

11-digit product format

636294492

Labeler code

63629

Product ID

63629-4492_6d6eead5-3d00-43ec-9736-6bb4d628ea95

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

levocetirizine dihydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA090385

Marketing category

ANDA

Marketing start

2011-02-25

Marketing end

0000-00-00

Substance

LEVOCETIRIZINE DIHYDROCHLORIDE

Active strength

5 mg/1

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