Acyclovir - 24236-590-24 - (Acyclovir)

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Drug Information of Acyclovir

Product NDC: 24236-590
Proprietary Name: Acyclovir
Non Proprietary Name: Acyclovir
Active Ingredient(s): 400    mg/1 & nbsp;   Acyclovir
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Acyclovir

Product NDC: 24236-590
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074578
Marketing Category: ANDA
Start Marketing Date: 20130227

Package Information of Acyclovir

Package NDC: 24236-590-24
Package Description: 24 CAPSULE in 1 CANISTER (24236-590-24)

NDC Information of Acyclovir

NDC Code 24236-590-24
Proprietary Name Acyclovir
Package Description 24 CAPSULE in 1 CANISTER (24236-590-24)
Product NDC 24236-590
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Acyclovir
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20130227
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name ACYCLOVIR
Strength Number 400
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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