Aspirin - 41250-535-76 - (Aspirin)

Alphabetical Index


Drug Information of Aspirin

Product NDC: 41250-535
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: 41250-535
Labeler Name: Meijer Distribution Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 19930826

Package Information of Aspirin

Package NDC: 41250-535-76
Package Description: 1 BOTTLE in 1 CARTON (41250-535-76) > 120 TABLET, DELAYED RELEASE in 1 BOTTLE

NDC Information of Aspirin

NDC Code 41250-535-76
Proprietary Name Aspirin
Package Description 1 BOTTLE in 1 CARTON (41250-535-76) > 120 TABLET, DELAYED RELEASE in 1 BOTTLE
Product NDC 41250-535
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Aspirin
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 19930826
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Meijer Distribution Inc
Substance Name ASPIRIN
Strength Number 81
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Aspirin


General Information