Sivextro Injection, Powder, Lyophilized, For Solution
Product Images NDC 67919-040

3 FDA label images from Merck Sharp & Dohme Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Sivextro (NDC 67919-040). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Merck Sharp & Dohme Llc, 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

Chemical Structure (Sivextro 01)

Chemical Structure (Sivextro 01)
Chemical structure diagram of tedizolid phosphate, the active ingredient in SIVEXTRO. The diagram shows the molecular formula with rings and functional groups connected by bonds, representing the chemical composition of the drug.*
FDA Label Image

Principal Display Panel (200 mg Tablet Blister Pack Carton)

Principal Display Panel (200 mg Tablet Blister Pack Carton)
SIVEXTRO (tedizolid phosphate) tablets packaging label for 200 mg per tablet strength. The label indicates 6 film-coated tablets per package and includes the NDC number 67919-041-02. It is a prescription-only oral tablet manufactured by Merck Sharp & Dohme LLC.*
FDA Label Image

Principal Display Panel (200 mg Vial Carton)

Principal Display Panel (200 mg Vial Carton)
Sivextro (tedizolid phosphate) for injection 200 mg per vial carton label for intravenous infusion. The package contains 10 single-use vials. It is labeled Rx only, sterile, and manufactured by Merck Sharp & Dohme LLC. The label includes storage instructions and warnings about incompatibility with solutions containing divalent cations like calcium and magnesium.*

* 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.