Cetirizine Hydrochloride

Product NDC
57451-5067
11-digit product format
574515067
Labeler code
57451
Product ID
57451-5067_6f2ce1a0-e50d-4feb-9b52-e70fca156c7e
Type
HUMAN OTC DRUG
Nonproprietary name
Cetirizine Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Ipca Laboratories Limited
Application
ANDA077498
Marketing category
ANDA
Marketing start
2007-12-27
Marketing end
0000-00-00
Substance
CETIRIZINE HYDROCHLORIDE
Active strength
10 mg/1
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
57451-5067-12024-12-24C16284748780-1960f7f55-d043-8e05-e053-dbdaa90a074a57293f46-e0ba-4f7b-a3f2-db1a798012cd
57451-5067-12019-10-29C16284748780-1960f7f55-d043-8e05-e053-dbdaa90a074a57293f46-e0ba-4f7b-a3f2-db1a798012cd