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VALACYCLOVIR HYDROCHLORIDE - 64679-152-01 - (VALACYCLOVIR HYDROCHLORIDE)

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Drug Information of VALACYCLOVIR HYDROCHLORIDE

Product NDC: 64679-152
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: 64679-152
Labeler Name: Wockhardt USA LLC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090216
Marketing Category: ANDA
Start Marketing Date: 20100524

Package Information of VALACYCLOVIR HYDROCHLORIDE

Package NDC: 64679-152-01
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (64679-152-01)

NDC Information of VALACYCLOVIR HYDROCHLORIDE

NDC Code 64679-152-01
Proprietary Name VALACYCLOVIR HYDROCHLORIDE
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (64679-152-01)
Product NDC 64679-152
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 Wockhardt USA 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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