Excedrin - 0067-2035-24 - (Acetaminophen, Asprin, Caffeine)

Alphabetical Index


Drug Information of Excedrin

Product NDC: 0067-2035
Proprietary Name: Excedrin
Non Proprietary Name: Acetaminophen, Asprin, Caffeine
Active Ingredient(s): 250; 250; 65    mg/1; mg/1; mg/1 & nbsp;   Acetaminophen, Asprin, Caffeine
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Excedrin

Product NDC: 0067-2035
Labeler Name: Novartis Consumer Health, Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA020802
Marketing Category: NDA
Start Marketing Date: 20110913

Package Information of Excedrin

Package NDC: 0067-2035-24
Package Description: 1 BOTTLE in 1 CARTON (0067-2035-24) > 24 TABLET, COATED in 1 BOTTLE

NDC Information of Excedrin

NDC Code 0067-2035-24
Proprietary Name Excedrin
Package Description 1 BOTTLE in 1 CARTON (0067-2035-24) > 24 TABLET, COATED in 1 BOTTLE
Product NDC 0067-2035
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Asprin, Caffeine
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20110913
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