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Phytonadione - 0548-1140-00 - (Phytonadione)

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Drug Information of Phytonadione

Product NDC: 0548-1140
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: 0548-1140
Labeler Name: Amphastar Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA083722
Marketing Category: ANDA
Start Marketing Date: 19880324

Package Information of Phytonadione

Package NDC: 0548-1140-00
Package Description: 25 SYRINGE in 1 CARTON (0548-1140-00) > .5 mL in 1 SYRINGE

NDC Information of Phytonadione

NDC Code 0548-1140-00
Proprietary Name Phytonadione
Package Description 25 SYRINGE in 1 CARTON (0548-1140-00) > .5 mL in 1 SYRINGE
Product NDC 0548-1140
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Phytonadione
Dosage Form Name INJECTION, EMULSION
Route Name PARENTERAL
Start Marketing Date 19880324
Marketing Category Name ANDA
Labeler Name Amphastar Pharmaceuticals, Inc.
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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