VALTREX - 55154-1114-9 - (valacyclovir hydrochloride)

Alphabetical Index


Drug Information of VALTREX

Product NDC: 55154-1114
Proprietary Name: VALTREX
Non Proprietary Name: valacyclovir hydrochloride
Active Ingredient(s): 500    mg/1 & nbsp;   valacyclovir hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of VALTREX

Product NDC: 55154-1114
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020487
Marketing Category: NDA
Start Marketing Date: 19950801

Package Information of VALTREX

Package NDC: 55154-1114-9
Package Description: 1260 TABLET, FILM COATED in 1 BOTTLE (55154-1114-9)

NDC Information of VALTREX

NDC Code 55154-1114-9
Proprietary Name VALTREX
Package Description 1260 TABLET, FILM COATED in 1 BOTTLE (55154-1114-9)
Product NDC 55154-1114
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name valacyclovir hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19950801
Marketing Category Name NDA
Labeler Name Cardinal Health
Substance Name VALACYCLOVIR HYDROCHLORIDE
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes DNA Polymerase Inhibitors [MoA],Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient]

Complete Information of VALTREX


General Information