Vyondys 53 Injection
Product Images NDC 60923-465

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Vyondys 53 (NDC 60923-465). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sarepta Therapeutics, 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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Chemical structure diagram of golodirsen, the active ingredient in Vyondys 53 injection by Sarepta Therapeutics. The image depicts the detailed molecular sequence of golodirsen, illustrating its nucleotide components and chemical bonds.*

FDA Label Image

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Vyondys 53 (golodirsen) Injection label showing the product name and generic name with an illustration of a vial. The label indicates an intravenous injection dosage form and is associated with Sarepta Therapeutics, Inc.*

FDA Label Image

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Label for Vyondys 53 (golodirsen) Injection 100 mg/2 mL (50 mg/mL) for intravenous infusion after dilution. Single-dose vial packaging contains 1 vial. The label includes storage instructions, manufacturer Sarepta Therapeutics, Inc., and active ingredient and excipient details per vial. The label displays product NDC 60923-465-02 and recommends using a 0.2 micron in-line filter during infusion.*

FDA Label Image

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Vyondys 53 (golodirsen) Injection label showing a strength of 100 mg per 2 mL (50 mg/mL), single dose vial, prescription only. Manufactured for Sarepta Therapeutics, Inc., Cambridge, MA. The label also includes a lot number and expiration date section and a barcode with the NDC 60923-465-02.*

* 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.