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