Ascriptin - 0067-0149-10 - (Aspirin)

Alphabetical Index


Drug Information of Ascriptin

Product NDC: 0067-0149
Proprietary Name: Ascriptin
Non Proprietary Name: Aspirin
Active Ingredient(s): 325    mg/1 & nbsp;   Aspirin
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Ascriptin

Product NDC: 0067-0149
Labeler Name: Novartis Consumer Health, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20090924

Package Information of Ascriptin

Package NDC: 0067-0149-10
Package Description: 1 BOTTLE in 1 CARTON (0067-0149-10) > 100 TABLET, FILM COATED in 1 BOTTLE

NDC Information of Ascriptin

NDC Code 0067-0149-10
Proprietary Name Ascriptin
Package Description 1 BOTTLE in 1 CARTON (0067-0149-10) > 100 TABLET, FILM COATED in 1 BOTTLE
Product NDC 0067-0149
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Aspirin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20090924
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Novartis Consumer Health, Inc.
Substance Name ASPIRIN
Strength Number 325
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Ascriptin


General Information