Cetirizine Hydrochloride

Product NDC

59556-769

11-digit product format

595560769

Labeler code

59556

Product ID

59556-769_ad90469d-d5d5-40e6-909f-455afde9034a

Type

HUMAN OTC DRUG

Nonproprietary name

Cetirizine Hydrochloride

Dosage form

CAPSULE, LIQUID FILLED

Route

ORAL

Labeler

Strides Pharma Inc

Application

ANDA205291

Marketing category

ANDA

Marketing start

2017-07-21

Marketing end

0000-00-00

Substance

CETIRIZINE HYDROCHLORIDE

Active strength

10 mg/1

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record