Oxycodone Hydrochloride Solution
Product Images NDC 67296-2167
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Oxycodone Hydrochloride (NDC 67296-2167). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Redpharm Drug, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Figure 1 (Oxycodone 02)
Principal Display Panel (30 mL Bottle Label)
This document contains information about Oxycodone Hydrochloride Oral Solution, with active ingredient of Oxycodone - Hydrochloride, USP 20mg. It includes details on inactive ingredients, dosage and administration instructions, storage guidelines, manufacturer details (Genus Lifesciences Inc.), and NDC code (64950-353-03). It is essential to keep this medication out of the reach of children.*
Principal Display Panel (500 mL Bottle Label)
This is a description of an oral solution containing Oxycodone Hydrochloride, USP. It comes in a strength of 5 mg per 5 mL and contains inactive ingredients such as citric acid, FD&C Red #40, natural/artificial berry flavor, purified water, sodium citrate dihydrate, sodium benzoate, saccharin sodium, and sorbitol. The dosage and administration details are provided in the accompanying prescribing information. This medication is manufactured by Genus Lifesciences Inc. in Allentown, PA. It is important to store this medication at 25°C (77°F) with excursions allowed to 15°- 30°C (59°-86°F) and to keep it out of reach of children. Each patient should be given the accompanying Medication Guide.*
Principal Display Panel (5 mL Cup Label)
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.