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Childrens TYLENOL - 50580-123-04 - (acetaminophen)

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Drug Information of Childrens TYLENOL

Product NDC: 50580-123
Proprietary Name: Childrens TYLENOL
Non Proprietary Name: acetaminophen
Active Ingredient(s): 160    mg/5mL & nbsp;   acetaminophen
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Childrens TYLENOL

Product NDC: 50580-123
Labeler Name: McNeil Consumer Healthcare Div. McNeil-PPC, Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20111101

Package Information of Childrens TYLENOL

Package NDC: 50580-123-04
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (50580-123-04) > 120 mL in 1 BOTTLE, PLASTIC

NDC Information of Childrens TYLENOL

NDC Code 50580-123-04
Proprietary Name Childrens TYLENOL
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (50580-123-04) > 120 mL in 1 BOTTLE, PLASTIC
Product NDC 50580-123
Product Type Name HUMAN OTC DRUG
Non Proprietary Name acetaminophen
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 20111101
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name McNeil Consumer Healthcare Div. McNeil-PPC, Inc
Substance Name ACETAMINOPHEN
Strength Number 160
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of Childrens TYLENOL


General Information