Vitamin K1 - 55154-2356-5 - (PHYTONADIONE)

Alphabetical Index


Drug Information of Vitamin K1

Product NDC: 55154-2356
Proprietary Name: Vitamin K1
Non Proprietary Name: PHYTONADIONE
Active Ingredient(s): 10    mg/mL & nbsp;   PHYTONADIONE
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, EMULSION
Coding System: National Drug Codes(NDC)

Labeler Information of Vitamin K1

Product NDC: 55154-2356
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA087955
Marketing Category: ANDA
Start Marketing Date: 20110824

Package Information of Vitamin K1

Package NDC: 55154-2356-5
Package Description: 5 AMPULE in 1 BAG (55154-2356-5) > 1 mL in 1 AMPULE

NDC Information of Vitamin K1

NDC Code 55154-2356-5
Proprietary Name Vitamin K1
Package Description 5 AMPULE in 1 BAG (55154-2356-5) > 1 mL in 1 AMPULE
Product NDC 55154-2356
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 10
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]

Complete Information of Vitamin K1


General Information