Allergy relief-D

Product NDC
49035-982
11-digit product format
490350982
Labeler code
49035
Product ID
49035-982_ef4fc264-bf2e-404d-95a0-ff92ed0bc347
Type
HUMAN OTC DRUG
Nonproprietary name
Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
EQUATE (WAL-MART STORES, INC.)
Application
ANDA090922
Marketing category
ANDA
Marketing start
2019-05-31
Marketing end
0000-00-00
Substance
CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
Active strength
5 mg/1; mg/1
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
64O047KTOACETIRIZINE HYDROCHLORIDE83881-52-1CETIRIZINE HYDROCHLORIDE
6V9V2RYJ8NPSEUDOEPHEDRINE HYDROCHLORIDE345-78-8PSEUDOEPHEDRINE HYDROCHLORIDE

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride Extended-Release Tablets, USPEQUATE (WAL-MART STORES, INC.) | Sun Pharmaceutical Industries Limited2019-05-23HUMAN OTC DRUG LABEL2