Acyclovir - 55289-629-30 - (Acyclovir)

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Drug Information of Acyclovir

Product NDC: 55289-629
Proprietary Name: Acyclovir
Non Proprietary Name: Acyclovir
Active Ingredient(s): 800    mg/1 & nbsp;   Acyclovir
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Acyclovir

Product NDC: 55289-629
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074556
Marketing Category: ANDA
Start Marketing Date: 20111207

Package Information of Acyclovir

Package NDC: 55289-629-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (55289-629-30)

NDC Information of Acyclovir

NDC Code 55289-629-30
Proprietary Name Acyclovir
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (55289-629-30)
Product NDC 55289-629
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Acyclovir
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111207
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name ACYCLOVIR
Strength Number 800
Strength Unit mg/1
Pharmaceutical Classes 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 [Chemical/Ingredient]

Complete Information of Acyclovir


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