TYLENOL - 50580-501-80 - (Acetaminophen)

Alphabetical Index


Drug Information of TYLENOL

Product NDC: 50580-501
Proprietary Name: TYLENOL
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 325    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: 50580-501
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: 19990201

Package Information of TYLENOL

Package NDC: 50580-501-80
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50580-501-80)

NDC Information of TYLENOL

NDC Code 50580-501-80
Proprietary Name TYLENOL
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50580-501-80)
Product NDC 50580-501
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19990201
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name McNeil Consumer Healthcare Div. McNeil-PPC, Inc
Substance Name ACETAMINOPHEN
Strength Number 325
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of TYLENOL


General Information