Home > National Drug Code (NDC) > childrens all day allergy

childrens all day allergy - 0904-5828-20 - (cetirizine hydrochloride)

Alphabetical Index


Drug Information of childrens all day allergy

Product NDC: 0904-5828
Proprietary Name: childrens 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 childrens all day allergy

Product NDC: 0904-5828
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA090254
Marketing Category: ANDA
Start Marketing Date: 20100726

Package Information of childrens all day allergy

Package NDC: 0904-5828-20
Package Description: 1 BOTTLE in 1 CARTON (0904-5828-20) > 118 mL in 1 BOTTLE

NDC Information of childrens all day allergy

NDC Code 0904-5828-20
Proprietary Name childrens all day allergy
Package Description 1 BOTTLE in 1 CARTON (0904-5828-20) > 118 mL in 1 BOTTLE
Product NDC 0904-5828
Product Type Name HUMAN OTC DRUG
Non Proprietary Name cetirizine hydrochloride
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20100726
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
Substance Name CETIRIZINE HYDROCHLORIDE
Strength Number 5
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of childrens all day allergy


General Information