acyclovir - 60505-5307-3 - (acyclovir)

Alphabetical Index


Drug Information of acyclovir

Product NDC: 60505-5307
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: 60505-5307
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077309
Marketing Category: ANDA
Start Marketing Date: 20060313

Package Information of acyclovir

Package NDC: 60505-5307-3
Package Description: 30 TABLET in 1 BOTTLE (60505-5307-3)

NDC Information of acyclovir

NDC Code 60505-5307-3
Proprietary Name acyclovir
Package Description 30 TABLET in 1 BOTTLE (60505-5307-3)
Product NDC 60505-5307
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name acyclovir
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20060313
Marketing Category Name ANDA
Labeler Name Apotex Corp.
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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