NDC 33261-491

Acyclovir

Acyclovir

Acyclovir is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Aidarex Pharmaceuticals Llc. The primary component is Acyclovir.

Product ID33261-491_7a30fb41-2a84-4afb-a155-46dba2cfb76a
NDC33261-491
Product TypeHuman Prescription Drug
Proprietary NameAcyclovir
Generic NameAcyclovir
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date1997-04-23
Marketing CategoryANDA / ANDA
Application NumberANDA074556
Labeler NameAidarex Pharmaceuticals LLC
Substance NameACYCLOVIR
Active Ingredient Strength400 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 FlagN
Listing Certified Through2019-12-31

Packaging

NDC 33261-491-28

28 TABLET in 1 BOTTLE (33261-491-28)
Marketing Start Date1997-04-23
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 33261-491-90 [33261049190]

Acyclovir TABLET
Marketing CategoryANDA
Application NumberANDA074556
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1997-04-23
Inactivation Date2020-01-31

NDC 33261-491-60 [33261049160]

Acyclovir TABLET
Marketing CategoryANDA
Application NumberANDA074556
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1997-04-23
Inactivation Date2020-01-31

NDC 33261-491-21 [33261049121]

Acyclovir TABLET
Marketing CategoryANDA
Application NumberANDA074556
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1997-04-23
Inactivation Date2020-01-31

NDC 33261-491-30 [33261049130]

Acyclovir TABLET
Marketing CategoryANDA
Application NumberANDA074556
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1997-04-23
Inactivation Date2020-01-31

NDC 33261-491-28 [33261049128]

Acyclovir TABLET
Marketing CategoryANDA
Application NumberANDA074556
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1997-04-23
Inactivation Date2020-01-31

NDC 33261-491-25 [33261049125]

Acyclovir TABLET
Marketing CategoryANDA
Application NumberANDA074556
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1997-04-23
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ACYCLOVIR400 mg/1

OpenFDA Data

SPL SET ID:68227df2-cac6-4799-8dcd-8c2f42204315
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 197311
  • 197310
  • 197313
  • 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]

    NDC Crossover Matching brand name "Acyclovir" or generic name "Acyclovir"

    NDCBrand NameGeneric Name
    0093-3630Acycloviracyclovir
    0093-8940AcyclovirAcyclovir
    0093-8943AcyclovirAcyclovir
    0093-8947AcyclovirAcyclovir
    0143-9657AcyclovirAcyclovir
    0143-9658AcyclovirAcyclovir
    0168-0825acycloviracyclovir
    0378-8700Acycloviracyclovir
    0378-8712AcyclovirAcyclovir
    0440-6030AcyclovirAcyclovir
    0440-7033acycloviracyclovir
    0472-0082AcyclovirAcyclovir
    0591-1159Acycloviracyclovir
    0713-0630AcyclovirAcyclovir
    0904-5789ACYCLOVIRACYCLOVIR
    0904-5790acycloviracyclovir
    10544-039Acycloviracyclovir
    10544-089Acycloviracyclovir
    10544-101AcyclovirAcyclovir
    68071-1841AcyclovirAcyclovir
    68071-3155AcyclovirAcyclovir
    68071-3222AcyclovirAcyclovir
    68071-4528AcyclovirAcyclovir
    68071-4559acycloviracyclovir
    68071-4345AcyclovirAcyclovir
    68084-109AcyclovirAcyclovir
    68084-108AcyclovirAcyclovir
    68071-4790AcyclovirAcyclovir
    68071-4799AcyclovirAcyclovir
    68084-107ACYCLOVIRACYCLOVIR
    68382-125acycloviracyclovir
    68382-049acycloviracyclovir
    68382-048acycloviracyclovir
    68382-668acycloviracyclovir
    68382-126acycloviracyclovir
    68382-792acycloviracyclovir
    68382-791acycloviracyclovir
    68382-992acycloviracyclovir
    68462-746acycloviracyclovir
    68788-6360acycloviracyclovir
    68788-0505AcyclovirAcyclovir
    68788-0504AcyclovirAcyclovir
    68788-0715AcyclovirAcyclovir
    68788-8989acycloviracyclovir
    68788-6827ACYCLOVIRACYCLOVIR
    68788-7382acycloviracyclovir
    68788-7378acycloviracyclovir
    68788-9783AcyclovirAcyclovir
    68788-7342AcyclovirAcyclovir
    68788-9690AcyclovirAcyclovir

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