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Tylenol Arthritis Pain - 50580-112-06 - (Acetaminophen)

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Drug Information of Tylenol Arthritis Pain

Product NDC: 50580-112
Proprietary Name: Tylenol Arthritis Pain
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 650    mg/1 & nbsp;   Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Tylenol Arthritis Pain

Product NDC: 50580-112
Labeler Name: McNeil Consumer Healthcare Div McNeil-PPC, Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA019872
Marketing Category: NDA
Start Marketing Date: 19981201

Package Information of Tylenol Arthritis Pain

Package NDC: 50580-112-06
Package Description: 3 POUCH in 1 CARTON (50580-112-06) > 2 TABLET, FILM COATED, EXTENDED RELEASE in 1 POUCH (50580-112-22)

NDC Information of Tylenol Arthritis Pain

NDC Code 50580-112-06
Proprietary Name Tylenol Arthritis Pain
Package Description 3 POUCH in 1 CARTON (50580-112-06) > 2 TABLET, FILM COATED, EXTENDED RELEASE in 1 POUCH (50580-112-22)
Product NDC 50580-112
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 19981201
Marketing Category Name NDA
Labeler Name McNeil Consumer Healthcare Div McNeil-PPC, Inc
Substance Name ACETAMINOPHEN
Strength Number 650
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Tylenol Arthritis Pain


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