Dilaudid Tablet
Product Images NDC 42858-122

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 Dilaudid (NDC 42858-122). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rhodes Pharmaceuticals Llc, 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

Chemical Structure (Dilaudid 01)

FDA Label Image

Principal Display Panel (2 mg Tablet Bottle Label)

Principal Display Panel (2 mg Tablet Bottle Label)
This appears to be a label for Dilaudid, which is a brand name for the medication hydromorphone. The label includes information such as the National Drug Code (NDC) number, manufacturer and marketer information, dosage instructions, and storage recommendations. It also includes a warning not to use the medication if the packaging is damaged.*
FDA Label Image

Principal Display Panel (4 mg Tablet Bottle Label)

FDA Label Image

Principal Display Panel (8 mg Tablet Bottle Label)

Principal Display Panel (8 mg Tablet Bottle Label)
This is a description of a pharmaceutical product. The product is marketed by Fodes Pharmaceuticals LP, located in Coventry, AI 02816. The product is manufactured by Hab Pharmaceutical Inc., located in Whippary, NJ 07981. The storage instructions recommend keeping the product at room temperature (20°-25°C or 68°-77°F) in a air-tight container as specified by USP. The text also includes some product codes and contact information for customer support.*
FDA Label Image

Principal Display Panel (473 mL Bottle Label)

Principal Display Panel (473 mL Bottle Label)
This is a description of Dilaudid® (hydromorphone HCl) oral solution, USP. It is a 5mg/5 mL (1 mg/mL) solution available in a one pint (473 mL) container. The NDC number for this product is 42858-416-16 and it is meant for prescription only. There are some details related to dosage and administration mentioned in the text, however, they are unclear due to errors.*

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