Acyclovir - 50383-810-16 - (Acyclovir)

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Drug Information of Acyclovir

Product NDC: 50383-810
Proprietary Name: Acyclovir
Non Proprietary Name: Acyclovir
Active Ingredient(s): 200    mg/5mL & nbsp;   Acyclovir
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Acyclovir

Product NDC: 50383-810
Labeler Name: Hi-Tech Pharmacal Co., Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077026
Marketing Category: ANDA
Start Marketing Date: 20050607

Package Information of Acyclovir

Package NDC: 50383-810-16
Package Description: 473 mL in 1 BOTTLE (50383-810-16)

NDC Information of Acyclovir

NDC Code 50383-810-16
Proprietary Name Acyclovir
Package Description 473 mL in 1 BOTTLE (50383-810-16)
Product NDC 50383-810
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Acyclovir
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 20050607
Marketing Category Name ANDA
Labeler Name Hi-Tech Pharmacal Co., Inc.
Substance Name ACYCLOVIR
Strength Number 200
Strength Unit mg/5mL
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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