Cidofovir - 67457-210-05 - (Cidofovir Anhydrous)

Alphabetical Index


Drug Information of Cidofovir

Product NDC: 67457-210
Proprietary Name: Cidofovir
Non Proprietary Name: Cidofovir Anhydrous
Active Ingredient(s): 75    mg/mL & nbsp;   Cidofovir Anhydrous
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Cidofovir

Product NDC: 67457-210
Labeler Name: Mylan Institutional LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201276
Marketing Category: ANDA
Start Marketing Date: 20130603

Package Information of Cidofovir

Package NDC: 67457-210-05
Package Description: 1 VIAL, GLASS in 1 CARTON (67457-210-05) > 5 mL in 1 VIAL, GLASS

NDC Information of Cidofovir

NDC Code 67457-210-05
Proprietary Name Cidofovir
Package Description 1 VIAL, GLASS in 1 CARTON (67457-210-05) > 5 mL in 1 VIAL, GLASS
Product NDC 67457-210
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cidofovir Anhydrous
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20130603
Marketing Category Name ANDA
Labeler Name Mylan Institutional LLC
Substance Name CIDOFOVIR
Strength Number 75
Strength Unit mg/mL
Pharmaceutical Classes Cytomegalovirus Nucleoside Analog DNA Polymerase Inhibitor [EPC],DNA Polymerase Inhibitors [MoA],Nucleoside Analog [Chemical/Ingredient]

Complete Information of Cidofovir


General Information