NDC 51660-904

VALACYCLOVIR

Valacyclovir Hydrochloride

VALACYCLOVIR is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Ohm Laboratories Inc.. The primary component is Valacyclovir Hydrochloride.

Product ID51660-904_623aa8f4-d84d-4dae-9fcb-51e2b288d52a
NDC51660-904
Product TypeHuman Prescription Drug
Proprietary NameVALACYCLOVIR
Generic NameValacyclovir Hydrochloride
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2009-11-25
Marketing CategoryANDA / ANDA
Application NumberANDA076588
Labeler NameOhm Laboratories Inc.
Substance NameVALACYCLOVIR HYDROCHLORIDE
Active Ingredient Strength500 mg/1
Pharm ClassesDNA 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 [EXT]
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 51660-904-90

90 TABLET in 1 BOTTLE (51660-904-90)
Marketing Start Date2009-11-25
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 51660-904-90 [51660090490]

VALACYCLOVIR TABLET
Marketing CategoryANDA
Application NumberANDA076588
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-11-25
Inactivation Date2020-01-31

NDC 51660-904-11 [51660090411]

VALACYCLOVIR TABLET
Marketing CategoryANDA
Application NumberANDA076588
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-11-25

NDC 51660-904-77 [51660090477]

VALACYCLOVIR TABLET
Marketing CategoryANDA
Application NumberANDA076588
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-11-25
Inactivation Date2020-01-31

NDC 51660-904-05 [51660090405]

VALACYCLOVIR TABLET
Marketing CategoryANDA
Application NumberANDA076588
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-11-25
Inactivation Date2020-01-31

NDC 51660-904-30 [51660090430]

VALACYCLOVIR TABLET
Marketing CategoryANDA
Application NumberANDA076588
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-11-25
Inactivation Date2020-01-31

NDC 51660-904-03 [51660090403]

VALACYCLOVIR TABLET
Marketing CategoryANDA
Application NumberANDA076588
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-11-25
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
VALACYCLOVIR HYDROCHLORIDE500 mg/1

OpenFDA Data

SPL SET ID:51f93a1c-90d0-4cbc-90f7-6f1415efd673
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 313564
  • 313565
    • UPC Code
  • 0351660905304

    • Pharmacological Class

    • 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 [EXT]

    Medicade Reported Pricing

    51660090430 VALACYCLOVIR HCL 500 MG TABLET

    Pricing Unit: EA | Drug Type:

    NDC Crossover Matching brand name "VALACYCLOVIR" or generic name "Valacyclovir Hydrochloride"

    NDCBrand NameGeneric Name
    0093-7258ValacyclovirValacyclovir
    0093-7259ValacyclovirValacyclovir
    68071-3135ValacyclovirValacyclovir
    68071-3276ValacyclovirValacyclovir
    68071-3372ValacyclovirValacyclovir
    68071-4805ValacyclovirValacyclovir
    68382-226ValacyclovirValacyclovir
    68382-225ValacyclovirValacyclovir
    70518-0323ValacyclovirValacyclovir
    70934-106ValacyclovirValacyclovir
    71335-0630ValacyclovirValacyclovir
    31722-704ValacyclovirValacyclovir
    31722-705ValacyclovirValacyclovir
    43063-771ValacyclovirValacyclovir
    43353-883ValacyclovirValacyclovir
    50090-2575ValacyclovirValacyclovir
    50090-2510ValacyclovirValacyclovir
    51660-904VALACYCLOVIRVALACYCLOVIR
    51660-905VALACYCLOVIRVALACYCLOVIR
    52343-051ValacyclovirValacyclovir
    52343-052ValacyclovirValacyclovir
    61919-066ValacyclovirValacyclovir
    61919-919ValacyclovirValacyclovir
    63187-950ValacyclovirValacyclovir
    63304-904ValacyclovirValacyclovir
    63304-905ValacyclovirValacyclovir
    65841-630ValacyclovirValacyclovir
    65841-629ValacyclovirValacyclovir
    61919-515VALACYCLOVIRVALACYCLOVIR
    63629-7958ValacyclovirValacyclovir
    50436-7050ValacyclovirValacyclovir
    50436-0704ValacyclovirValacyclovir
    70518-2402ValacyclovirValacyclovir
    68071-3332ValacyclovirValacyclovir
    0378-4275Valacyclovir Hydrochloridevalacyclovir
    0378-4276Valacyclovir Hydrochloridevalacyclovir
    0781-5208Valacyclovir HydrochlorideValacyclovir Hydrochloride
    0781-5209Valacyclovir HydrochlorideValacyclovir Hydrochloride
    0904-6565Valacyclovir HydrochlorideValacyclovir Hydrochloride
    10544-937valacyclovir hydrochloridevalacyclovir hydrochloride
    16714-697Valacyclovir HydrochlorideValacyclovir Hydrochloride
    0173-0565VALTREXvalacyclovir hydrochloride
    0173-0933VALTREXvalacyclovir hydrochloride
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