Levocetirizine Dihydrochloride

Product NDC

68788-6892

11-digit product format

687886892

Labeler code

68788

Product ID

68788-6892_4a58d869-e01c-418e-8136-690d7b6f9ab7

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Levocetirizine Dihydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Preferred Pharmaceuticals Inc.

Application

ANDA203027

Marketing category

ANDA

Marketing start

2017-02-13

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