EXCEDRIN - 0067-2039-24 - (Acetaminophen, Aspirin (NSAID) and Caffeine)

Alphabetical Index


Drug Information of EXCEDRIN

Product NDC: 0067-2039
Proprietary Name: EXCEDRIN
Non Proprietary Name: Acetaminophen, Aspirin (NSAID) and Caffeine
Active Ingredient(s): 250; 250; 65    mg/1; mg/1; mg/1 & nbsp;   Acetaminophen, Aspirin (NSAID) and Caffeine
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of EXCEDRIN

Product NDC: 0067-2039
Labeler Name: Novartis Consumer Health, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA020802
Marketing Category: NDA
Start Marketing Date: 20100215

Package Information of EXCEDRIN

Package NDC: 0067-2039-24
Package Description: 1 BOTTLE in 1 CARTON (0067-2039-24) > 24 TABLET, FILM COATED in 1 BOTTLE

NDC Information of EXCEDRIN

NDC Code 0067-2039-24
Proprietary Name EXCEDRIN
Package Description 1 BOTTLE in 1 CARTON (0067-2039-24) > 24 TABLET, FILM COATED in 1 BOTTLE
Product NDC 0067-2039
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Aspirin (NSAID) and Caffeine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100215
Marketing Category Name NDA
Labeler Name Novartis Consumer Health, Inc.
Substance Name ACETAMINOPHEN; ASPIRIN; CAFFEINE
Strength Number 250; 250; 65
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of EXCEDRIN


General Information