Acyclovir - 49349-521-08 - (Acyclovir)

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Drug Information of Acyclovir

Product NDC: 49349-521
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: 49349-521
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074556
Marketing Category: ANDA
Start Marketing Date: 20110920

Package Information of Acyclovir

Package NDC: 49349-521-08
Package Description: 10 TABLET in 1 BLISTER PACK (49349-521-08)

NDC Information of Acyclovir

NDC Code 49349-521-08
Proprietary Name Acyclovir
Package Description 10 TABLET in 1 BLISTER PACK (49349-521-08)
Product NDC 49349-521
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Acyclovir
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110920
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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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