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Pain Relief - 41250-046-90 - (Acetaminophen)

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Drug Information of Pain Relief

Product NDC: 41250-046
Proprietary Name: Pain Relief
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 Pain Relief

Product NDC: 41250-046
Labeler Name: Meijer Distribution Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20090818

Package Information of Pain Relief

Package NDC: 41250-046-90
Package Description: 500 TABLET, COATED in 1 BOTTLE (41250-046-90)

NDC Information of Pain Relief

NDC Code 41250-046-90
Proprietary Name Pain Relief
Package Description 500 TABLET, COATED in 1 BOTTLE (41250-046-90)
Product NDC 41250-046
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20090818
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Meijer Distribution Inc
Substance Name ACETAMINOPHEN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Pain Relief


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