Acyclovir - 61442-111-01 - (Acyclovir)

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Drug Information of Acyclovir

Product NDC: 61442-111
Proprietary Name: Acyclovir
Non Proprietary Name: Acyclovir
Active Ingredient(s): 200    mg/1 & nbsp;   Acyclovir
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Acyclovir

Product NDC: 61442-111
Labeler Name: Carlsbad Technology, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075090
Marketing Category: ANDA
Start Marketing Date: 20091022

Package Information of Acyclovir

Package NDC: 61442-111-01
Package Description: 100 CAPSULE in 1 BOTTLE, PLASTIC (61442-111-01)

NDC Information of Acyclovir

NDC Code 61442-111-01
Proprietary Name Acyclovir
Package Description 100 CAPSULE in 1 BOTTLE, PLASTIC (61442-111-01)
Product NDC 61442-111
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Acyclovir
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20091022
Marketing Category Name ANDA
Labeler Name Carlsbad Technology, Inc.
Substance Name ACYCLOVIR
Strength Number 200
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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