NDC 50090-0644

Acyclovir

Acyclovir

Acyclovir is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by A-s Medication Solutions. The primary component is Acyclovir.

Product ID50090-0644_0c62fccb-8ff3-4079-8661-0b5bf292f0f7
NDC50090-0644
Product TypeHuman Prescription Drug
Proprietary NameAcyclovir
Generic NameAcyclovir
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2009-10-22
Marketing CategoryANDA / ANDA
Application NumberANDA075382
Labeler NameA-S Medication Solutions
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 Through2023-12-31

Packaging

NDC 50090-0644-2

25 TABLET in 1 BOTTLE (50090-0644-2)
Marketing Start Date2014-11-28
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 50090-0644-2 [50090064402]

Acyclovir TABLET
Marketing CategoryANDA
Application NumberANDA075382
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-11-28
Marketing End Date2018-07-31

NDC 50090-0644-6 [50090064406]

Acyclovir TABLET
Marketing CategoryANDA
Application NumberANDA075382
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-11-28
Marketing End Date2018-07-31

NDC 50090-0644-5 [50090064405]

Acyclovir TABLET
Marketing CategoryANDA
Application NumberANDA075382
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-11-28
Marketing End Date2019-08-31

NDC 50090-0644-9 [50090064409]

Acyclovir TABLET
Marketing CategoryANDA
Application NumberANDA075382
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-11-28
Marketing End Date2019-08-31

NDC 50090-0644-3 [50090064403]

Acyclovir TABLET
Marketing CategoryANDA
Application NumberANDA075382
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-11-28
Marketing End Date2018-07-31

NDC 50090-0644-4 [50090064404]

Acyclovir TABLET
Marketing CategoryANDA
Application NumberANDA075382
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-11-28
Marketing End Date2019-08-31

Drug Details

Active Ingredients

IngredientStrength
ACYCLOVIR400 mg/1

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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