Acyclovir - 63323-105-10 - (ACYCLOVIR SODIUM)

Alphabetical Index


Drug Information of Acyclovir

Product NDC: 63323-105
Proprietary Name: Acyclovir
Non Proprietary Name: ACYCLOVIR SODIUM
Active Ingredient(s): 50    mg/mL & nbsp;   ACYCLOVIR SODIUM
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Acyclovir

Product NDC: 63323-105
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075015
Marketing Category: ANDA
Start Marketing Date: 20001017

Package Information of Acyclovir

Package NDC: 63323-105-10
Package Description: 10 VIAL in 1 TRAY (63323-105-10) > 10 mL in 1 VIAL

NDC Information of Acyclovir

NDC Code 63323-105-10
Proprietary Name Acyclovir
Package Description 10 VIAL in 1 TRAY (63323-105-10) > 10 mL in 1 VIAL
Product NDC 63323-105
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ACYCLOVIR SODIUM
Dosage Form Name INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20001017
Marketing Category Name ANDA
Labeler Name APP Pharmaceuticals, LLC
Substance Name ACYCLOVIR SODIUM
Strength Number 50
Strength Unit mg/mL
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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