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Childrens Pain Relief - 59779-452-01 - (Acetaminophen)

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Drug Information of Childrens Pain Relief

Product NDC: 59779-452
Proprietary Name: Childrens Pain Relief
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 80    mg/1 & nbsp;   Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET, CHEWABLE
Coding System: National Drug Codes(NDC)

Labeler Information of Childrens Pain Relief

Product NDC: 59779-452
Labeler Name: WOONSOCKET PRESCRIPTION CENTER,INCORPORATED
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20041206

Package Information of Childrens Pain Relief

Package NDC: 59779-452-01
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (59779-452-01) > 30 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC

NDC Information of Childrens Pain Relief

NDC Code 59779-452-01
Proprietary Name Childrens Pain Relief
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (59779-452-01) > 30 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC
Product NDC 59779-452
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET, CHEWABLE
Route Name ORAL
Start Marketing Date 20041206
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name WOONSOCKET PRESCRIPTION CENTER,INCORPORATED
Substance Name ACETAMINOPHEN
Strength Number 80
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Childrens Pain Relief


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