LEVOCETIRIZINE DIHYDROCHLORIDE

Product NDC

50090-2061

11-digit product format

500902061

Labeler code

50090

Product ID

50090-2061_356a58a7-d0c5-4598-810b-9d3a3877a724

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

levocetirizine dihydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

A-S Medication Solutions

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