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valacyclovir hydrochloride - 59746-324-37 - (valacyclovir hydrochloride)

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Drug Information of valacyclovir hydrochloride

Product NDC: 59746-324
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: 59746-324
Labeler Name: Jubilant Cadista Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201506
Marketing Category: ANDA
Start Marketing Date: 20120405

Package Information of valacyclovir hydrochloride

Package NDC: 59746-324-37
Package Description: 250 TABLET, FILM COATED in 1 BOTTLE (59746-324-37)

NDC Information of valacyclovir hydrochloride

NDC Code 59746-324-37
Proprietary Name valacyclovir hydrochloride
Package Description 250 TABLET, FILM COATED in 1 BOTTLE (59746-324-37)
Product NDC 59746-324
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name valacyclovir hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120405
Marketing Category Name ANDA
Labeler Name Jubilant Cadista Pharmaceuticals Inc.
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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