Aspirin - 11534-155-11 - (Aspirin)

Alphabetical Index


Drug Information of Aspirin

Product NDC: 11534-155
Proprietary Name: Aspirin
Non Proprietary Name: Aspirin
Active Ingredient(s): 81    mg/1 & nbsp;   Aspirin
Administration Route(s): ORAL
Dosage Form(s): TABLET, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Aspirin

Product NDC: 11534-155
Labeler Name: Sunrise Pharmaceutical Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100103

Package Information of Aspirin

Package NDC: 11534-155-11
Package Description: 120 TABLET, DELAYED RELEASE in 1 BOTTLE (11534-155-11)

NDC Information of Aspirin

NDC Code 11534-155-11
Proprietary Name Aspirin
Package Description 120 TABLET, DELAYED RELEASE in 1 BOTTLE (11534-155-11)
Product NDC 11534-155
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Aspirin
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20100103
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Sunrise Pharmaceutical Inc
Substance Name ASPIRIN
Strength Number 81
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Aspirin


General Information