Home > National Drug Code (NDC) > Valacyclovir Hydrochloride

Valacyclovir Hydrochloride - 21695-965-04 - (Valacyclovir Hydrochloride)

Alphabetical Index


Drug Information of Valacyclovir Hydrochloride

Product NDC: 21695-965
Proprietary Name: Valacyclovir Hydrochloride
Non Proprietary Name: Valacyclovir Hydrochloride
Active Ingredient(s): 1    g/1 & nbsp;   Valacyclovir Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Valacyclovir Hydrochloride

Product NDC: 21695-965
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077135
Marketing Category: ANDA
Start Marketing Date: 20100611

Package Information of Valacyclovir Hydrochloride

Package NDC: 21695-965-04
Package Description: 4 TABLET, FILM COATED in 1 BOTTLE (21695-965-04)

NDC Information of Valacyclovir Hydrochloride

NDC Code 21695-965-04
Proprietary Name Valacyclovir Hydrochloride
Package Description 4 TABLET, FILM COATED in 1 BOTTLE (21695-965-04)
Product NDC 21695-965
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Valacyclovir Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100611
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name VALACYCLOVIR HYDROCHLORIDE
Strength Number 1
Strength Unit g/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 Valacyclovir Hydrochloride


General Information