Benadryl - 66715-9706-1 - (Diphenhydramine Hydrochloride)

Alphabetical Index


Drug Information of Benadryl

Product NDC: 66715-9706
Proprietary Name: Benadryl
Non Proprietary Name: Diphenhydramine Hydrochloride
Active Ingredient(s): 25    mg/1 & nbsp;   Diphenhydramine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Benadryl

Product NDC: 66715-9706
Labeler Name: Lil' Drug Store Products, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100916

Package Information of Benadryl

Package NDC: 66715-9706-1
Package Description: 1 POUCH in 1 CARTON (66715-9706-1) > 2 TABLET, FILM COATED in 1 POUCH

NDC Information of Benadryl

NDC Code 66715-9706-1
Proprietary Name Benadryl
Package Description 1 POUCH in 1 CARTON (66715-9706-1) > 2 TABLET, FILM COATED in 1 POUCH
Product NDC 66715-9706
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Diphenhydramine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100916
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Lil' Drug Store Products, Inc.
Substance Name DIPHENHYDRAMINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Benadryl


General Information