Acyclovir - 54868-5687-0 - (acyclovir)

Alphabetical Index


Drug Information of Acyclovir

Product NDC: 54868-5687
Proprietary Name: Acyclovir
Non Proprietary Name: acyclovir
Active Ingredient(s): 200    mg/5mL & nbsp;   acyclovir
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Acyclovir

Product NDC: 54868-5687
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077026
Marketing Category: ANDA
Start Marketing Date: 20061003

Package Information of Acyclovir

Package NDC: 54868-5687-0
Package Description: 473 mL in 1 BOTTLE (54868-5687-0)

NDC Information of Acyclovir

NDC Code 54868-5687-0
Proprietary Name Acyclovir
Package Description 473 mL in 1 BOTTLE (54868-5687-0)
Product NDC 54868-5687
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name acyclovir
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 20061003
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name ACYCLOVIR
Strength Number 200
Strength Unit mg/5mL
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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