Nytol - 10158-043-04 - (diphenhydramine HCl)

Alphabetical Index


Drug Information of Nytol

Product NDC: 10158-043
Proprietary Name: Nytol
Non Proprietary Name: diphenhydramine HCl
Active Ingredient(s): 25    mg/1 & nbsp;   diphenhydramine HCl
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Nytol

Product NDC: 10158-043
Labeler Name: GlaxoSmithKline consumer Healthcare LP
Product Type: HUMAN OTC DRUG
FDA Application Number: part338
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20110812

Package Information of Nytol

Package NDC: 10158-043-04
Package Description: 4 BLISTER PACK in 1 CARTON (10158-043-04) > 8 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Nytol

NDC Code 10158-043-04
Proprietary Name Nytol
Package Description 4 BLISTER PACK in 1 CARTON (10158-043-04) > 8 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 10158-043
Product Type Name HUMAN OTC DRUG
Non Proprietary Name diphenhydramine HCl
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110812
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 Nytol


General Information