NDC 12634-697

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 ID12634-697_271bf420-cc51-52eb-e054-00144ff8d46c
NDC12634-697
Product TypeHuman Prescription Drug
Proprietary Nameacyclovir
Generic NameAcyclovir
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2006-03-13
Marketing CategoryANDA / ANDA
Application NumberANDA077309
Labeler NameApotheca Inc.
Substance NameACYCLOVIR
Active Ingredient Strength800 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 12634-697-65

5 TABLET in 1 BLISTER PACK (12634-697-65)
Marketing Start Date2006-03-13
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 12634-697-61 [12634069761]

acyclovir TABLET
Marketing CategoryANDA
Application NumberANDA077309
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-03-13
Inactivation Date2020-01-31

NDC 12634-697-65 [12634069765]

acyclovir TABLET
Marketing CategoryANDA
Application NumberANDA077309
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-03-13
Inactivation Date2020-01-31

NDC 12634-697-55 [12634069755]

acyclovir TABLET
Marketing CategoryANDA
Application NumberANDA077309
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-03-13
Inactivation Date2020-01-31

NDC 12634-697-54 [12634069754]

acyclovir TABLET
Marketing CategoryANDA
Application NumberANDA077309
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-03-13
Inactivation Date2020-01-31

NDC 12634-697-90 [12634069790]

acyclovir TABLET
Marketing CategoryANDA
Application NumberANDA077309
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-03-13
Inactivation Date2020-01-31

NDC 12634-697-01 [12634069701]

acyclovir TABLET
Marketing CategoryANDA
Application NumberANDA077309
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-03-13
Inactivation Date2020-01-31

NDC 12634-697-91 [12634069791]

acyclovir TABLET
Marketing CategoryANDA
Application NumberANDA077309
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-03-13
Inactivation Date2020-01-31

NDC 12634-697-09 [12634069709]

acyclovir TABLET
Marketing CategoryANDA
Application NumberANDA077309
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-03-13
Inactivation Date2020-01-31

NDC 12634-697-79 [12634069779]

acyclovir TABLET
Marketing CategoryANDA
Application NumberANDA077309
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-03-13
Inactivation Date2020-01-31

NDC 12634-697-71 [12634069771]

acyclovir TABLET
Marketing CategoryANDA
Application NumberANDA077309
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-03-13
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ACYCLOVIR800 mg/1

OpenFDA Data

SPL SET ID:271bfbb6-4990-500a-e054-00144ff8d46c
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 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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