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Pain Reliever - 70253-175-12 - (Acetaminophen)

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Drug Information of Pain Reliever

Product NDC: 70253-175
Proprietary Name: Pain Reliever
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 Pain Reliever

Product NDC: 70253-175
Labeler Name: NASH-FINCH COMPANY
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 19930402

Package Information of Pain Reliever

Package NDC: 70253-175-12
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (70253-175-12) > 100 TABLET in 1 BOTTLE, PLASTIC

NDC Information of Pain Reliever

NDC Code 70253-175-12
Proprietary Name Pain Reliever
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (70253-175-12) > 100 TABLET in 1 BOTTLE, PLASTIC
Product NDC 70253-175
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19930402
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name NASH-FINCH COMPANY
Substance Name ACETAMINOPHEN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Pain Reliever


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