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Extra Strength Pain Reliever - 0363-0175-29 - (Acetaminophen)

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Drug Information of Extra Strength Pain Reliever

Product NDC: 0363-0175
Proprietary Name: Extra Strength 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 Extra Strength Pain Reliever

Product NDC: 0363-0175
Labeler Name: WALGREEN CO.
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 19930402

Package Information of Extra Strength Pain Reliever

Package NDC: 0363-0175-29
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (0363-0175-29) > 150 TABLET in 1 BOTTLE, PLASTIC

NDC Information of Extra Strength Pain Reliever

NDC Code 0363-0175-29
Proprietary Name Extra Strength Pain Reliever
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (0363-0175-29) > 150 TABLET in 1 BOTTLE, PLASTIC
Product NDC 0363-0175
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 WALGREEN CO.
Substance Name ACETAMINOPHEN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Extra Strength Pain Reliever


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