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Naloxone Hydrochloride Injection, Solution
Product Images NDC 70069-072
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Product Visual Gallery
This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Naloxone Hydrochloride (NDC 70069-072). 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.
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This is a prescription drug with the NDC code 70069-072-01. It is a sterile solution of Naloxone Hydrochloride with Sodium Chloride added in appropriate proportion to adjust tonicity. The pH of the solution is adjusted to 4.0 using hydrochloride and the preservatives used are Methylparaben and Propylparaben. It is stored within the temperature range of 20°C to 25°C (68°F to 77°F). The drug is meant for intravenous, intramuscular, or subcutaneous use, and the recommended dosage can be found in the package insert. This solution comes in a 10 mL multi-dose vial and was manufactured in India for Somerset Therapeutics, LLC. The Lot and Exp can be overprinted in the blank area, and the vial must be discarded after a certain date.*
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This is a description of a pharmaceutical drug called Naloxone Hydrochloride Injection, USP. It comes in a 4 mg/10 mL vial with a concentration of 0.4 mg/mL and can be administered through intravenous, intramuscular, or subcutaneous routes. The medication contains naloxone hydrochloride, methylparaben, and HO for pH adjustment. The recommended dosage is as indicated on the packaging and the drug should be stored at 20-55°C in a controlled room temperature environment. The drug is sterile, non-pyrogenic, and should be protected from light until use. The manufacturer is Somerset Mgt L and the drug is only available with a prescription.*
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This is a description for Naloxone Hydrochloride Injection, used for Intravenous, Intramuscular, or Subcutaneous use, manufactured by Somerset Therapeutics, LLC. Each mL contains 0.4 mg of naloxone hydrochloride and preservatives methyiparaben 1.8 mg and propylparaben 0.2 mg. It also includes sodium chloride for tonicity adjustment and may contain HGI for pH adjustment. This sterile and nonpyrogeric injection is available in 10 x 10 mL multiple-dose vials, and should be stored at controlled room temperature and protected from light. NDC 70069-072-10.*
* 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.
