Cetrizine Hydrochloride

Product NDC
0904-6372
11-digit product format
009046372
Labeler code
0904
Product ID
0904-6372_7f720ea2-ce48-46fd-e053-2991aa0a71ea
Type
HUMAN OTC DRUG
Nonproprietary name
CETIRIZINE HYDROCHLORIDE
Dosage form
SOLUTION
Route
ORAL
Labeler
Major Pharmaceuticals
Application
ANDA090474
Marketing category
ANDA
Marketing start
2014-02-24
Marketing end
0000-00-00
Substance
CETIRIZINE HYDROCHLORIDE
Active strength
1 mg/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0904-6372-20ML - Milliliter0904-63728b8a2056-5e5d-40f2-8de5-ebce1e76dce712014-06-03