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TYLENOL Extra Strength - 50580-449-09 - (Acetaminophen)

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Drug Information of TYLENOL Extra Strength

Product NDC: 50580-449
Proprietary Name: TYLENOL Extra Strength
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 500    mg/1 & nbsp;   Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of TYLENOL Extra Strength

Product NDC: 50580-449
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: 19840819

Package Information of TYLENOL Extra Strength

Package NDC: 50580-449-09
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (50580-449-09) > 100 TABLET, COATED in 1 BOTTLE, PLASTIC

NDC Information of TYLENOL Extra Strength

NDC Code 50580-449-09
Proprietary Name TYLENOL Extra Strength
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (50580-449-09) > 100 TABLET, COATED in 1 BOTTLE, PLASTIC
Product NDC 50580-449
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 19840819
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 Extra Strength


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