TYLENOL - 50580-422-50 - (Acetaminophen)

Alphabetical Index


Drug Information of TYLENOL

Product NDC: 50580-422
Proprietary Name: TYLENOL
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 500    mg/1 & nbsp;   Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of TYLENOL

Product NDC: 50580-422
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: 20050701

Package Information of TYLENOL

Package NDC: 50580-422-50
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (50580-422-50) > 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

NDC Information of TYLENOL

NDC Code 50580-422-50
Proprietary Name TYLENOL
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (50580-422-50) > 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product NDC 50580-422
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20050701
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name McNeil Consumer Healthcare Div. McNeil-PPC, Inc
Substance Name ACETAMINOPHEN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of TYLENOL


General Information