Product Images Naloxone Hydrochloride
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Product Label Images
The following 4 images provide visual information about the product associated with Naloxone Hydrochloride NDC 70069-072 by Somerset Therapeutics, Llc, such as packaging, labeling, and the appearance of the drug itself. This resource could be helpful for medical professionals, pharmacists, and patients seeking to verify medication information and ensure they have the correct product.
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.*
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.*
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.*
* The product label images have been analyzed using a combination of traditional computing and machine learning techniques. It should be noted that the descriptions provided may not be entirely accurate as they are experimental in nature. Use the information in this page at your own discretion and risk.