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all day allergy - 30142-974-26 - (cetirizine hydrochloride)

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Drug Information of all day allergy

Product NDC: 30142-974
Proprietary Name: all day allergy
Non Proprietary Name: cetirizine hydrochloride
Active Ingredient(s): 5    mg/5mL & nbsp;   cetirizine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of all day allergy

Product NDC: 30142-974
Labeler Name: Kroger Company
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA090254
Marketing Category: ANDA
Start Marketing Date: 20080508

Package Information of all day allergy

Package NDC: 30142-974-26
Package Description: 1 BOTTLE in 1 CARTON (30142-974-26) > 120 mL in 1 BOTTLE

NDC Information of all day allergy

NDC Code 30142-974-26
Proprietary Name all day allergy
Package Description 1 BOTTLE in 1 CARTON (30142-974-26) > 120 mL in 1 BOTTLE
Product NDC 30142-974
Product Type Name HUMAN OTC DRUG
Non Proprietary Name cetirizine hydrochloride
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20080508
Marketing Category Name ANDA
Labeler Name Kroger Company
Substance Name CETIRIZINE HYDROCHLORIDE
Strength Number 5
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of all day allergy


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