Benadryl - 50580-226-51 - (Diphenhydramine Hydrochloride)

Alphabetical Index


Drug Information of Benadryl

Product NDC: 50580-226
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: 50580-226
Labeler Name: McNeil Consumer Healthcare Div McNeil-PPC, Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20080901

Package Information of Benadryl

Package NDC: 50580-226-51
Package Description: 2 BLISTER PACK in 1 CARTON (50580-226-51) > 12 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Benadryl

NDC Code 50580-226-51
Proprietary Name Benadryl
Package Description 2 BLISTER PACK in 1 CARTON (50580-226-51) > 12 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 50580-226
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Diphenhydramine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20080901
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name McNeil Consumer Healthcare Div McNeil-PPC, Inc
Substance Name DIPHENHYDRAMINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Benadryl


General Information