Oxycodone Hydrochloride Solution
Product Images NDC 43386-920

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Oxycodone Hydrochloride (NDC 43386-920). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lupin Pharmaceuticals, Inc., 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

Carton

Packaging label for Oxycodone Hydrochloride oral solution, USP, 100 mg/5 mL (20 mg/mL) in a 30 mL bottle. The label includes dosing instructions, a caution about the solution being highly concentrated, and notes that it is for patients who are opioid tolerant. It is manufactured by Lupin Pharmaceuticals, Inc. and is prescription-only (Rx only). The label also displays the product NDC 43386-920-60.*

FDA Label Image

Container

Label for Oxycodone Hydrochloride Oral Solution, USP 20 mg/mL in a 30 mL bottle, manufactured by Lupin Pharmaceuticals, Inc. The label indicates the product is for oral use and is only for use in patients who are opioid tolerant. It includes dosing information, inactive ingredients, storage instructions, and safety warnings about keeping medication out of reach of children.*

FDA Label Image

Fig 1

An instructional diagram showing a dosing syringe for oral Oxycodone Hydrochloride solution, labeled with volume markings (0.25 to 1.0 mL) and corresponding milligram dosages (5 to 20 mg). It emphasizes measuring the dose from the widest portion of the plunger, not the narrow tip.*

FDA Label Image

Structure

Chemical structure depicting the molecular composition of oxycodone hydrochloride, showing the arrangement of its rings and functional groups including hydroxy, methyl, and methoxy substituents along with the hydrochloride ion.*

* 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.