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Extra Strength Pain Relief - 55910-531-08 - (Acetaminophen)

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Drug Information of Extra Strength Pain Relief

Product NDC: 55910-531
Proprietary Name: Extra Strength Pain Relief
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 500    mg/1 & nbsp;   Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Extra Strength Pain Relief

Product NDC: 55910-531
Labeler Name: DOLGENCORP, LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20051211

Package Information of Extra Strength Pain Relief

Package NDC: 55910-531-08
Package Description: 1 BOTTLE in 1 CARTON (55910-531-08) > 24 TABLET in 1 BOTTLE

NDC Information of Extra Strength Pain Relief

NDC Code 55910-531-08
Proprietary Name Extra Strength Pain Relief
Package Description 1 BOTTLE in 1 CARTON (55910-531-08) > 24 TABLET in 1 BOTTLE
Product NDC 55910-531
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20051211
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name DOLGENCORP, LLC
Substance Name ACETAMINOPHEN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Extra Strength Pain Relief


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