Phytonadione Injection, Emulsion
Product Images NDC 0404-9969

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Phytonadione (NDC 0404-9969). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Henry Schein, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

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FDA Label Image

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Phytonadione Injectable Emulsion, USP is a medication used for Hemorrhagic Disease of the Newborn Prophylaxis and Anticoagulant-Induced Prothrombin Deficiency. The recommended dosage for newborns is 0.5 to 1 mg IM within 1 hour of birth for prophylaxis, while for adults, the initial dosage ranges from 2.5 mg to 10 mg or up to 25 mg for Anticoagulant-Induced Prothrombin Deficiency caused by coumarin or indanedione derivatives. For Hypoprothrombinemia Due to other causes, the dosage ranges from 2.5 mg to 25 mg or more, rarely up to 50 ma. More details can be found in the circular text.*

FDA Label Image

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This is a product description for two different package types of the drug Phytonadione. One package type is a carton containing 25 ampules of 1 mL each, with National Drug Code (NDC) 43598-40!. The other package type is a single ampule containing an injectable emulsion concentration of 10mg/1mL, with NDC 43598-405-11.*

FDA Label Image

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* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.