Oxycodone Hydrochloride
Product Images NDC 17856-0393

3 FDA label images from Atlantic Biologicals Corps · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Oxycodone Hydrochloride (NDC 17856-0393). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Atlantic Biologicals Corps, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Label Image (17856 0393)

Label Image (17856 0393)
Oxycodone Hydrochloride 10 mg per 0.5 mL oral solution syringe, 0.5 mL unit dose delivered in an oral syringe. Labeler is Atlantic Biologicals Corps. The label includes dosage instructions, storage conditions, handling precautions, and contact information for questions or comments. The product NDC is 17856-0393.*
FDA Label Image

Chemical Structure (Bd5f1a52 A044 42b5 A733 A0145b72c5bc 01)

Chemical Structure (Bd5f1a52 A044 42b5 A733 A0145b72c5bc 01)
Chemical structure diagram of Oxycodone Hydrochloride showing the molecular arrangement of the compound with specific functional groups, including hydroxyl, methoxy, and amide groups, along with the hydrochloride component indicated.*
FDA Label Image

Figure 1 Syringe Diagram (Bd5f1a52 A044 42b5 A733 A0145b72c5bc 02)

Figure 1 Syringe Diagram (Bd5f1a52 A044 42b5 A733 A0145b72c5bc 02)
An instructional diagram of an oral syringe showing dosage measurements ranging from 2 mg to 20 mg with corresponding volumes from 0.1 mL to 1 mL. Labels indicate how to measure the dose using the widest portion of the plunger and cautions against measuring to the narrow tip.*

* 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.