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Naloxone Hydrochloride Injection, Solution
Product Images NDC 70069-071
View Photos of 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 Naloxone Hydrochloride (NDC 70069-071). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Somerset Therapeutics, 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.
Product Images & Figures Index
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This is a prescription drug identified by its national drug code (NDC) as 70069-071-01, containing Naloxone Hydrochloride in 0.4 mg/mL concentration, and intended for intravenous, intramuscular or subcutaneous usage. The product is a 1 mL single-dose vial that should be protected from light. The manufacturer of the drug is Somerset Therapeutics, LLC, located in Hollywood, FL, and manufactured in India under code No. KRIDRUGS/KTK/28/289/97. The product has a no-varnish area and is labeled as ST-NLX11/L/04.*
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This is a medication called Naloxone Hydrochloride for intravenous, intramuscular or subcutaneous use. Each vial contains 0.4 mg of Naloxone Hydrochloride and sodium chloride. The medication may contain Hydrochloric Acid for pH adjustment. The product should be stored at a temperature between 20°C to 25°C and protected from light. It is manufactured by Somerset Therapeutics LLC, and the usual dosage is indicated in the package insert. The text also gives instructions for aseptic technique and warns against reusing unused portions.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
