Naloxone Hydrochloride Injection
Product Images NDC 76329-3369

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Naloxone Hydrochloride (NDC 76329-3369). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by International Medication Systems, Limited, 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

Instructions (Instructions)

This text provides instructions on how to prepare a vial for injection. It advises the reader to remove protective caps and align the vial so that the injector needle is correctly positioned. The user is then advised to thread the vial into the injector in three half turns, remove the needle and expel air before carrying out the injection. The reader is warned not to push the vial into the injector, as this could cause misalignment.*

FDA Label Image

Structure (Structure)

FDA Label Image

Carton 1469

The text is a list of a drug called "NALOXONE HYDROCHLORIDE INJ., USP" with a concentration of "@ mg/mL".*

FDA Label Image

Carton 3369

This is a description of a medication product that contains naloxone hydrochloride. It comes in a single dose and the package should be protected from light and stored at room temperature. The medication is used as an antipodal antagonist and is in injection form. It contains 1mg of naloxone hydrochloride and 5.35mg of sodium chloride. The medication is non-pyroganic and non-toxic, and the package should not be opened until ready to use. The product is manufactured by International Medication Systems in the USA.*

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