NDC 12634-520

Acyclovir

Acyclovir

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

Product ID12634-520_34f57b50-d012-2c77-e054-00144ff88e88
NDC12634-520
Product TypeHuman Prescription Drug
Proprietary NameAcyclovir
Generic NameAcyclovir
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date1997-04-23
Marketing CategoryANDA / ANDA
Application NumberANDA074556
Labeler NameApotheca Inc.
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 12634-520-40

40 TABLET in 1 BOTTLE (12634-520-40)
Marketing Start Date1997-04-23
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 12634-520-78 [12634052078]

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

NDC 12634-520-09 [12634052009]

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

NDC 12634-520-66 [12634052066]

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

NDC 12634-520-81 [12634052081]

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

NDC 12634-520-69 [12634052069]

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

NDC 12634-520-60 [12634052060]

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

NDC 12634-520-59 [12634052059]

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

NDC 12634-520-71 [12634052071]

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

NDC 12634-520-63 [12634052063]

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

NDC 12634-520-61 [12634052061]

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

NDC 12634-520-40 [12634052040]

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

NDC 12634-520-80 [12634052080]

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

NDC 12634-520-01 [12634052001]

Acyclovir TABLET
Marketing CategoryANDA
Application NumberANDA074556
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1997-07-22
Inactivation Date2020-01-31

NDC 12634-520-94 [12634052094]

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

NDC 12634-520-79 [12634052079]

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

NDC 12634-520-52 [12634052052]

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

NDC 12634-520-74 [12634052074]

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

NDC 12634-520-57 [12634052057]

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

NDC 12634-520-82 [12634052082]

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

NDC 12634-520-85 [12634052085]

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

NDC 12634-520-00 [12634052000]

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

NDC 12634-520-54 [12634052054]

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

NDC 12634-520-91 [12634052091]

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

NDC 12634-520-95 [12634052095]

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

NDC 12634-520-67 [12634052067]

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

NDC 12634-520-96 [12634052096]

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:34f57b50-d013-2c77-e054-00144ff88e88
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 197311

    • 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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