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Phytonadione - 76329-1240-5 - (Phytonadione)

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Drug Information of Phytonadione

Product NDC: 76329-1240
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)

Labeler Information of Phytonadione

Product NDC: 76329-1240
Labeler Name: International Medication Systems, Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA083722
Marketing Category: ANDA
Start Marketing Date: 20030418

Package Information of Phytonadione

Package NDC: 76329-1240-5
Package Description: 25 SYRINGE in 1 CARTON (76329-1240-5) > .5 mL in 1 SYRINGE

NDC Information of Phytonadione

NDC Code 76329-1240-5
Proprietary Name Phytonadione
Package Description 25 SYRINGE in 1 CARTON (76329-1240-5) > .5 mL in 1 SYRINGE
Product NDC 76329-1240
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 International Medication Systems, Limited
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]

Complete Information of Phytonadione


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