Product NDC: | 55154-2388 |
Proprietary Name: | Vitamin K1 |
Non Proprietary Name: | PHYTONADIONE |
Active Ingredient(s): | 2 mg/mL & nbsp; PHYTONADIONE |
Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
Dosage Form(s): | INJECTION, EMULSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55154-2388 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA087954 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110824 |
Package NDC: | 55154-2388-5 |
Package Description: | 5 AMPULE in 1 BAG (55154-2388-5) > .5 mL in 1 AMPULE |
NDC Code | 55154-2388-5 |
Proprietary Name | Vitamin K1 |
Package Description | 5 AMPULE in 1 BAG (55154-2388-5) > .5 mL in 1 AMPULE |
Product NDC | 55154-2388 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | PHYTONADIONE |
Dosage Form Name | INJECTION, EMULSION |
Route Name | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
Start Marketing Date | 20110824 |
Marketing Category Name | ANDA |
Labeler Name | Cardinal Health |
Substance Name | PHYTONADIONE |
Strength Number | 2 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Increased Prothrombin Activity [PE],Reversed Anticoagulation Activity [PE],Vitamin K [Chemical/Ingredient],Vitamin K [EPC],Warfarin Reversal Agent [EPC] |