Phytonadione Injection, Emulsion
Product Images NDC 51662-1698

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Phytonadione (NDC 51662-1698). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hf Acquisition Co Llc, Dba Healthfirst, 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

Structure (51662 1698 Structure)

Chemical structure diagram of phytonadione, illustrating its molecular arrangement with aromatic rings and side chains consistent with its chemical identity.*

FDA Label Image

Table (51662 1698 Table 1)

A dosing information table for Phytonadione injection detailing recommended dosages for newborns and adults. The table includes dosage specifics for newborn prophylaxis, treatment, and adult indications such as anticoagulant-induced prothrombin deficiency and hypoprothrombinemia due to other causes.*

FDA Label Image

Label (51662 1698 2 Pouch)

Label for PHYTONADIONE injectable emulsion, USP, with a strength of 10 mg per 1 mL in a 1 mL ampule. The label includes the NDC number 51662-1698-2, lot number 789210, and expiration date 2030-09-19. It indicates use for intramuscular, subcutaneous, or intravenous administration and storage instructions. The label also states it is distributed by HF Acquisition Co., LLC.*

FDA Label Image

Label (51662 1698 2 Case)

Label for PHYTONADIONE Injectable Emulsion USP, 10 mg/mL in a 1 mL ampule, sold as a case of 25. The label includes the NDC 51662-1698-3, lot number 789210, and expiration date 2030-09-19. Distributed by HF Acquisition Co., LLC, Mukilteo, WA. Contains storage and handling information.*

FDA Label Image

Label (51662 1698 Source)

Phytonadione Injectable Emulsion, USP 10 mg/mL carton label for 25 single-dose ampules. The label indicates the product is for intramuscular, subcutaneous, or intravenous use. The labeler shown is Dr. Reddy's with distributor Dr. Reddy's Laboratories Inc., Princeton, NJ, and the product is made in India. The label includes storage instructions and a barcode.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.