Acyclovir - 21695-011-35 - (acyclovir)

Alphabetical Index


Drug Information of Acyclovir

Product NDC: 21695-011
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: 21695-011
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA074980
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 19981030

Package Information of Acyclovir

Package NDC: 21695-011-35
Package Description: 35 TABLET in 1 BOTTLE (21695-011-35)

NDC Information of Acyclovir

NDC Code 21695-011-35
Proprietary Name Acyclovir
Package Description 35 TABLET in 1 BOTTLE (21695-011-35)
Product NDC 21695-011
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name acyclovir
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19981030
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Rebel Distributors 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


General Information