Allergy relief-D

Product NDC
11822-9994
Type
HUMAN OTC DRUG
Nonproprietary name
Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
RITE AID
Application
ANDA090922
Marketing category
ANDA
Substance
CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
11822-9994-12 BLISTER PACK in 1 CARTON (11822-9994-1) / 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK20230720NoHistorical
11822-9994-26 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (11822-9994-2) 20230720NoHistorical

Related DailyMed Labels

Set IDTitleManufacturerEffective dateTypeVersion
1bf7c028-1648-4211-8847-84cce833a0f1Allergy relief-DRITE AID | Sun Pharmaceutical Industries Limited2025-01-02HUMAN OTC DRUG LABEL3