Oxycodone Hydrochloride
Product Images NDC 17856-0826

8 FDA label images from Atlantic Biologicals Corp. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Oxycodone Hydrochloride (NDC 17856-0826). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Atlantic Biologicals Corp., 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

Image Description (17856 0826 01 Overwrap)

Image Description (17856 0826 01 Overwrap)
Label for Oxycodone Hydrochloride oral syringe, 100 mg/5 mL concentration, delivering 10 mg per 0.5 mL dose. The label includes manufacturing details, expiration date (08/15/2021), batch numbers, and is distributed by Atlantic Biologicals Corp. A barcode is shown at the bottom.*
FDA Label Image

Image Description (17856 0826 01)

Image Description (17856 0826 01)
Label for Oxycodone Hydrochloride oral solution, 10 mg per 0.5 mL, packaged as 60 syringes. The label indicates storage at controlled room temperature (20° to 25°C). It includes a barcode, GTIN, serial number, expiration date (10/26/21), lot number, and DEA Schedule II classification. Packaged by Unit Dose Solutions and distributed by Atlantic Biologicals Corp.*
FDA Label Image

Image Description (17856 0826 02 Overwrap)

Image Description (17856 0826 02 Overwrap)
Label for Oxycodone Hydrochloride oral syringe, 100 mg/5 mL concentration, with a dosage indication of 2.5 mg per 0.125 mL. The syringe delivers 0.125 mL. Manufactured by PAI and distributed by Atlantic Biologicals Corp. Includes lot numbers and an expiration date of 10/09/2021.*
FDA Label Image

Image Description (17856 0826 02)

Image Description (17856 0826 02)
Label for Oxycodone Hydrochloride oral solution dosed 2.5 mg per 0.125 mL, packaged as 60 syringes. Label includes storage instructions at 20° to 25°C and warns to keep out of reach of children. Distributed by Atlantic Biologicals Corp. and packaged by Unit Dose Solutions.*
FDA Label Image

Image Description (17856 0826 03)

Image Description (17856 0826 03)
Label for Oxycodone Hydrochloride oral solution, 20 mg per 1 mL, in a 120 syringe package by Atlantic Biologicals Corp. Storage instructions indicate controlled room temperature (20° to 25°C). The label includes a barcode, GTIN, serial number, expiration date (10/26/21), lot number, and a controlled substance schedule II (CII) designation.*
FDA Label Image

Image Description (17856 0826 04)

Image Description (17856 0826 04)
Label for Oxycodone Hydrochloride oral solution 20 mg per 1 mL, delivered in 1 mL unit doses. The product is packaged as 60 syringes by Unit Dose Solutions and distributed by Atlantic Biologicals Corp. Storage instructions specify controlled room temperature (20° to 25°C). The label includes lot, expiration date, serial numbers, and a reorder phone number.*
FDA Label Image

Image Description (17856 0826 05)

Image Description (17856 0826 05)
Label for OXYCODONE HYDROCHLORIDE oral solution 5 mg per 0.25 mL by Atlantic Biologicals Corp. The label states a quantity of 120 syringes, storage instructions at 20° to 25°C, and includes barcodes, a QR code, and regulatory information such as Controlled Substance Schedule CII.*
FDA Label Image

Chemical Structure (Oxycodone 01)

Chemical Structure (Oxycodone 01)
Chemical structure of oxycodone hydrochloride depicting the arrangement of its molecular components, including aromatic rings and hydroxyl groups, with associated hydrochloride indicated.*

* 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.