Cetirizine Hydrochloride

Product NDC

13668-590

11-digit product format

136680590

Labeler code

13668

Product ID

13668-590_8efccd14-c6c9-460b-b20f-5b9b3bd34a79

Type

HUMAN OTC DRUG

Nonproprietary name

Cetirizine Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Torrent Pharmaceuticals Limited

Application

ANDA079191

Marketing category

ANDA

Marketing start

2010-04-15

Marketing end

0000-00-00

Substance

CETIRIZINE HYDROCHLORIDE

Active strength

5 mg/1

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record