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Regular Strength Aspirin EC - 0904-2013-72 - (Aspirin)

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Drug Information of Regular Strength Aspirin EC

Product NDC: 0904-2013
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: 0904-2013
Labeler Name: Major Pharmaceuticals 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: 0904-2013-72
Package Description: 300 TABLET, DELAYED RELEASE in 1 BOTTLE (0904-2013-72)

NDC Information of Regular Strength Aspirin EC

NDC Code 0904-2013-72
Proprietary Name Regular Strength Aspirin EC
Package Description 300 TABLET, DELAYED RELEASE in 1 BOTTLE (0904-2013-72)
Product NDC 0904-2013
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 Major Pharmaceuticals Inc
Substance Name ASPIRIN
Strength Number 325
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Regular Strength Aspirin EC


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