Excedrin - 0067-2053-83 - (Acetaminophen, Diphenhydramine Citrate)

Alphabetical Index


Drug Information of Excedrin

Product NDC: 0067-2053
Proprietary Name: Excedrin
Non Proprietary Name: Acetaminophen, Diphenhydramine Citrate
Active Ingredient(s): 500; 38    mg/1; mg/1 & nbsp;   Acetaminophen, Diphenhydramine Citrate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Excedrin

Product NDC: 0067-2053
Labeler Name: Novartis Consumer Health, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100301

Package Information of Excedrin

Package NDC: 0067-2053-83
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (0067-2053-83) > 125 TABLET in 1 BOTTLE, PLASTIC

NDC Information of Excedrin

NDC Code 0067-2053-83
Proprietary Name Excedrin
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (0067-2053-83) > 125 TABLET in 1 BOTTLE, PLASTIC
Product NDC 0067-2053
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Diphenhydramine Citrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100301
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Novartis Consumer Health, Inc.
Substance Name ACETAMINOPHEN; DIPHENHYDRAMINE CITRATE
Strength Number 500; 38
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Excedrin


General Information