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Valacyclovir Hydrochloride - 59762-8399-1 - (Valacyclovir Hydrochloride)

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Drug Information of Valacyclovir Hydrochloride

Product NDC: 59762-8399
Proprietary Name: Valacyclovir Hydrochloride
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 Valacyclovir Hydrochloride

Product NDC: 59762-8399
Labeler Name: Greenstone LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090682
Marketing Category: ANDA
Start Marketing Date: 20100524

Package Information of Valacyclovir Hydrochloride

Package NDC: 59762-8399-1
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (59762-8399-1)

NDC Information of Valacyclovir Hydrochloride

NDC Code 59762-8399-1
Proprietary Name Valacyclovir Hydrochloride
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (59762-8399-1)
Product NDC 59762-8399
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Valacyclovir Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100524
Marketing Category Name ANDA
Labeler Name Greenstone LLC
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 Valacyclovir Hydrochloride


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