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VALACYCLOVIR HYDROCHLORIDE - 68084-634-21 - (VALACYCLOVIR HYDROCHLORIDE)

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Drug Information of VALACYCLOVIR HYDROCHLORIDE

Product NDC: 68084-634
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: 68084-634
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090216
Marketing Category: ANDA
Start Marketing Date: 20121129

Package Information of VALACYCLOVIR HYDROCHLORIDE

Package NDC: 68084-634-21
Package Description: 3 BLISTER PACK in 1 CARTON (68084-634-21) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68084-634-11)

NDC Information of VALACYCLOVIR HYDROCHLORIDE

NDC Code 68084-634-21
Proprietary Name VALACYCLOVIR HYDROCHLORIDE
Package Description 3 BLISTER PACK in 1 CARTON (68084-634-21) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68084-634-11)
Product NDC 68084-634
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name VALACYCLOVIR HYDROCHLORIDE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20121129
Marketing Category Name ANDA
Labeler Name American Health Packaging
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


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