EXCEDRIN - 0067-6238-06 - (Acetaminophen, Aspirin)

Alphabetical Index


Drug Information of EXCEDRIN

Product NDC: 0067-6238
Proprietary Name: EXCEDRIN
Non Proprietary Name: Acetaminophen, Aspirin
Active Ingredient(s): 250; 250    mg/1; mg/1 & nbsp;   Acetaminophen, Aspirin
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of EXCEDRIN

Product NDC: 0067-6238
Labeler Name: Novartis Consumer Health, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100215

Package Information of EXCEDRIN

Package NDC: 0067-6238-06
Package Description: 1 BOTTLE in 1 CARTON (0067-6238-06) > 6 TABLET, FILM COATED in 1 BOTTLE

NDC Information of EXCEDRIN

NDC Code 0067-6238-06
Proprietary Name EXCEDRIN
Package Description 1 BOTTLE in 1 CARTON (0067-6238-06) > 6 TABLET, FILM COATED in 1 BOTTLE
Product NDC 0067-6238
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Aspirin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100215
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Novartis Consumer Health, Inc.
Substance Name ACETAMINOPHEN; ASPIRIN
Strength Number 250; 250
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of EXCEDRIN


General Information