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Regular Strength Aspirin EC - 52959-018-20 - (Aspirin)

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Drug Information of Regular Strength Aspirin EC

Product NDC: 52959-018
Proprietary Name: Regular Strength Aspirin EC
Non Proprietary Name: Aspirin
Active Ingredient(s): 325    mg/1 & nbsp;   Aspirin
Administration Route(s): ORAL
Dosage Form(s): TABLET, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Regular Strength Aspirin EC

Product NDC: 52959-018
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20110909

Package Information of Regular Strength Aspirin EC

Package NDC: 52959-018-20
Package Description: 20 TABLET, DELAYED RELEASE in 1 BOTTLE (52959-018-20)

NDC Information of Regular Strength Aspirin EC

NDC Code 52959-018-20
Proprietary Name Regular Strength Aspirin EC
Package Description 20 TABLET, DELAYED RELEASE in 1 BOTTLE (52959-018-20)
Product NDC 52959-018
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Aspirin
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20110909
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name H.J. Harkins Company, Inc.
Substance Name ASPIRIN
Strength Number 325
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Regular Strength Aspirin EC


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