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Up and Up all day allergy relief d - 11673-176-62 - (Cetirizine HCl, Pseudoephedrine HCl)

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Drug Information of Up and Up all day allergy relief d

Product NDC: 11673-176
Proprietary Name: Up and Up all day allergy relief d
Non Proprietary Name: Cetirizine HCl, Pseudoephedrine HCl
Active Ingredient(s): 5; 120    mg/1; mg/1 & nbsp;   Cetirizine HCl, Pseudoephedrine HCl
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Up and Up all day allergy relief d

Product NDC: 11673-176
Labeler Name: Target Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA077170
Marketing Category: ANDA
Start Marketing Date: 20090728

Package Information of Up and Up all day allergy relief d

Package NDC: 11673-176-62
Package Description: 4 BLISTER PACK in 1 CARTON (11673-176-62) > 6 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

NDC Information of Up and Up all day allergy relief d

NDC Code 11673-176-62
Proprietary Name Up and Up all day allergy relief d
Package Description 4 BLISTER PACK in 1 CARTON (11673-176-62) > 6 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC 11673-176
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Cetirizine HCl, Pseudoephedrine HCl
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20090728
Marketing Category Name ANDA
Labeler Name Target Corporation
Substance Name CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
Strength Number 5; 120
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Up and Up all day allergy relief d


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