Sominex - 0135-0057-11 - (diphenhydramine HCl)

Alphabetical Index


Drug Information of Sominex

Product NDC: 0135-0057
Proprietary Name: Sominex
Non Proprietary Name: diphenhydramine HCl
Active Ingredient(s): 25    mg/1 & nbsp;   diphenhydramine HCl
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Sominex

Product NDC: 0135-0057
Labeler Name: GlaxoSmithKline Consumer Healthcare LP
Product Type: HUMAN OTC DRUG
FDA Application Number: part338
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20101108

Package Information of Sominex

Package NDC: 0135-0057-11
Package Description: 32 TABLET in 1 BLISTER PACK (0135-0057-11)

NDC Information of Sominex

NDC Code 0135-0057-11
Proprietary Name Sominex
Package Description 32 TABLET in 1 BLISTER PACK (0135-0057-11)
Product NDC 0135-0057
Product Type Name HUMAN OTC DRUG
Non Proprietary Name diphenhydramine HCl
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101108
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name GlaxoSmithKline Consumer Healthcare LP
Substance Name DIPHENHYDRAMINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Sominex


General Information