Product NDC: | 55154-3952 |
Proprietary Name: | Phytonadione |
Non Proprietary Name: | Phytonadione |
Active Ingredient(s): | 1 mg/.5mL & nbsp; Phytonadione |
Administration Route(s): | PARENTERAL |
Dosage Form(s): | INJECTION, EMULSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55154-3952 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA083722 |
Marketing Category: | ANDA |
Start Marketing Date: | 20030418 |
Package NDC: | 55154-3952-5 |
Package Description: | 5 SYRINGE in 1 BAG (55154-3952-5) > .5 mL in 1 SYRINGE |
NDC Code | 55154-3952-5 |
Proprietary Name | Phytonadione |
Package Description | 5 SYRINGE in 1 BAG (55154-3952-5) > .5 mL in 1 SYRINGE |
Product NDC | 55154-3952 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Phytonadione |
Dosage Form Name | INJECTION, EMULSION |
Route Name | PARENTERAL |
Start Marketing Date | 20030418 |
Marketing Category Name | ANDA |
Labeler Name | Cardinal Health |
Substance Name | PHYTONADIONE |
Strength Number | 1 |
Strength Unit | mg/.5mL |
Pharmaceutical Classes | Increased Prothrombin Activity [PE],Reversed Anticoagulation Activity [PE],Vitamin K [Chemical/Ingredient],Vitamin K [EPC],Warfarin Reversal Agent [EPC] |