Aspirin - 57344-080-01 - (ASPIRIN)

Alphabetical Index


Drug Information of Aspirin

Product NDC: 57344-080
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: 57344-080
Labeler Name: AAA Pharmaceutical, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20121215

Package Information of Aspirin

Package NDC: 57344-080-01
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (57344-080-01) > 120 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC

NDC Information of Aspirin

NDC Code 57344-080-01
Proprietary Name Aspirin
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (57344-080-01) > 120 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC
Product NDC 57344-080
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ASPIRIN
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20121215
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name AAA Pharmaceutical, Inc.
Substance Name ASPIRIN
Strength Number 81
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Aspirin


General Information