Acyclovir - 55289-273-10 - (Acyclovir)

Alphabetical Index


Drug Information of Acyclovir

Product NDC: 55289-273
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: 55289-273
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074578
Marketing Category: ANDA
Start Marketing Date: 19970423

Package Information of Acyclovir

Package NDC: 55289-273-10
Package Description: 10 CAPSULE in 1 BOTTLE, PLASTIC (55289-273-10)

NDC Information of Acyclovir

NDC Code 55289-273-10
Proprietary Name Acyclovir
Package Description 10 CAPSULE in 1 BOTTLE, PLASTIC (55289-273-10)
Product NDC 55289-273
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Acyclovir
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19970423
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


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