Acyclovir - 43063-204-05 - (acyclovir)

Alphabetical Index


Drug Information of Acyclovir

Product NDC: 43063-204
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: 43063-204
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074727
Marketing Category: ANDA
Start Marketing Date: 20100323

Package Information of Acyclovir

Package NDC: 43063-204-05
Package Description: 5 CAPSULE in 1 BOTTLE, PLASTIC (43063-204-05)

NDC Information of Acyclovir

NDC Code 43063-204-05
Proprietary Name Acyclovir
Package Description 5 CAPSULE in 1 BOTTLE, PLASTIC (43063-204-05)
Product NDC 43063-204
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name acyclovir
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20100323
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, 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


General Information