NDC 62756-915

Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride

Cetirizine Hydrochloride And Pseudoephedrine Hydrochloride

Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride is a Oral Tablet, Film Coated, Extended Release in the Human Otc Drug category. It is labeled and distributed by Sun Pharmaceutical Industries, Inc.. The primary component is Cetirizine Hydrochloride; Pseudoephedrine Hydrochloride.

Product ID62756-915_69aa4eab-3b98-49a3-b0eb-d34411e61e0d
NDC62756-915
Product TypeHuman Otc Drug
Proprietary NameCetirizine Hydrochloride and Pseudoephedrine Hydrochloride
Generic NameCetirizine Hydrochloride And Pseudoephedrine Hydrochloride
Dosage FormTablet, Film Coated, Extended Release
Route of AdministrationORAL
Marketing Start Date2012-09-29
Marketing CategoryANDA / ANDA
Application NumberANDA090922
Labeler NameSun Pharmaceutical Industries, Inc.
Substance NameCETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
Active Ingredient Strength5 mg/1; mg/1
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 62756-915-62

2 BLISTER PACK in 1 CARTON (62756-915-62) > 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (62756-915-60)
Marketing Start Date2012-09-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 62756-915-83 [62756091583]

Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA090922
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-09-29

NDC 62756-915-73 [62756091573]

Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA090922
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-09-29

NDC 62756-915-62 [62756091562]

Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA090922
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-09-29

NDC 62756-915-63 [62756091563]

Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA090922
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-09-29

Drug Details

Active Ingredients

IngredientStrength
CETIRIZINE HYDROCHLORIDE5 mg/1

OpenFDA Data

SPL SET ID:796c4b81-145b-4050-a851-dec81ff97006
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1014571
  • NDC Crossover Matching brand name "Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride" or generic name "Cetirizine Hydrochloride And Pseudoephedrine Hydrochloride"

    NDCBrand NameGeneric Name
    45802-147Cetirizine hydrochloride and Pseudoephedrine hydrochlorideCetirizine hydrochloride, Pseudoephedrine hydrochloride
    45802-721Cetirizine Hydrochloride and Pseudoephedrine HydrochlorideCetirizine HCl, Pseudoephedrine HCl
    50090-1098Cetirizine Hydrochloride and Pseudoephedrine HydrochlorideCetirizine HCl, Pseudoephedrine HCl
    62756-915Cetirizine Hydrochloride and Pseudoephedrine HydrochlorideCetirizine Hydrochloride and Pseudoephedrine Hydrochloride
    63187-955Cetirizine Hydrochloride and Pseudoephedrine HydrochlorideCetirizine HCl, Pseudoephedrine HCl
    63868-964Cetirizine Hydrochloride and Pseudoephedrine HydrochlorideCetirizine Hydrochloride and Pseudoephedrine Hydrochloride
    68258-8907Cetirizine Hydrochloride and Pseudoephedrine HydrochlorideCetirizine HCl, Pseudoephedrine HCl
    70677-0146all day allergy-DCetirizine Hydrochloride and Pseudoephedrine Hydrochloride
    49035-982Allergy relief-DCetirizine Hydrochloride and Pseudoephedrine Hydrochloride
    51660-940Allergy relief-DCetirizine Hydrochloride and Pseudoephedrine Hydrochloride
    68016-531Allergy relief-DCetirizine Hydrochloride and Pseudoephedrine Hydrochloride
    69842-994Allergy Relief-DCetirizine hydrochloride and pseudoephedrine hydrochloride
    70000-0163Allergy relief-DCetirizine Hydrochloride and Pseudoephedrine Hydrochloride
    0363-0989Wal-Zyr DCetirizine Hydrochloride and Pseudoephedrine Hydrochloride
    50580-728ZYRTEC-DCetirizine Hydrochloride and Pseudoephedrine Hydrochloride

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