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Leader Arthritis Pain Reliever - 37205-034-71 - (Acetaminophen)

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Drug Information of Leader Arthritis Pain Reliever

Product NDC: 37205-034
Proprietary Name: Leader Arthritis Pain Reliever
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 Leader Arthritis Pain Reliever

Product NDC: 37205-034
Labeler Name: Cardinal Health
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076200
Marketing Category: ANDA
Start Marketing Date: 20020430

Package Information of Leader Arthritis Pain Reliever

Package NDC: 37205-034-71
Package Description: 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (37205-034-71)

NDC Information of Leader Arthritis Pain Reliever

NDC Code 37205-034-71
Proprietary Name Leader Arthritis Pain Reliever
Package Description 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (37205-034-71)
Product NDC 37205-034
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20020430
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name ACETAMINOPHEN
Strength Number 650
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Leader Arthritis Pain Reliever


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