Naloxone Hydrochloride Injection, Solution
Product Images NDC 51662-1544

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Naloxone Hydrochloride (NDC 51662-1544). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hf Acquisition Co Llc, Dba Healthfirst, 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

Serialized Labeling (51662 1544 1 Serialized Labeling)

This is a prescription medicine provided in a single-dose vial with a concentration of 0.4 mg per mL. The identification number and code are included on the package in addition to information on the manufacturer and the package insert. It is distributed by HF Acquisition Co., LLC located in Washington (WA), United States. No other details are available.*

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Vial Label (51662 1544 1 Vial Label)

This is a prescription drug with NDC 55150-327-01 for intravenous or intramuscular use. It contains Naloxone Hydrochloride and each milliliter of the injection contains 0.4 mg of the drug. The manufacturer of the drug is AuroMedics Pharma LLC and it is packed in a single-dose vial. The text provides a code of TS/DRUGS/13/2010___P1421609.*

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51662 1544 2 Pouch Labeling

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51662 1544 3 Case Labeling

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51662 1544 3 Rfid Case Labeling Update

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Structure (Structure)

This appears to be a product label for Naloxone Hydrochloride, which is a medication used to counteract the effects of opioids, especially in cases of opioid overdose. The label provides information about the chemical structure and formula of the drug.*

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Vial Labeling

This is a description for a medication called Naloxone Hydrochloride designed for intravenous and intramuscular use only. It comes in a 1mL single-dose vial with a concentration of 0.4mg per mL. The medication is manufactured by AuroMedics Pharma LLC and should be protected from light. The NDC number for this product is 55150-327-01. No other information about the medication's uses, benefits or side effects is provided.*

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