Acyclovir - 0378-8700-06 - (acyclovir)

Alphabetical Index


Drug Information of Acyclovir

Product NDC: 0378-8700
Proprietary Name: Acyclovir
Non Proprietary Name: acyclovir
Active Ingredient(s): 50    mg/g & nbsp;   acyclovir
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Acyclovir

Product NDC: 0378-8700
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202459
Marketing Category: ANDA
Start Marketing Date: 20130507

Package Information of Acyclovir

Package NDC: 0378-8700-06
Package Description: 1 TUBE in 1 CARTON (0378-8700-06) > 15 g in 1 TUBE

NDC Information of Acyclovir

NDC Code 0378-8700-06
Proprietary Name Acyclovir
Package Description 1 TUBE in 1 CARTON (0378-8700-06) > 15 g in 1 TUBE
Product NDC 0378-8700
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name acyclovir
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20130507
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
Substance Name ACYCLOVIR
Strength Number 50
Strength Unit mg/g
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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