Hydromorphone Hydrochloride
Product Images NDC 67296-1642

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Hydromorphone Hydrochloride (NDC 67296-1642). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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

Chemical-structure (Hydromorphone Hydrochloride Tablets Usp 1)

FDA Label Image

Label (Hydromorphone)

Label (Hydromorphone)
NDC 67296-1642-9 is a prescription drug called HYDROMORPHONE HCL C. It is available in a package of 24 tablets, each containing 2mg of the active ingredient. This lot of HYDROMORPHONE HCL C has a manufacturing date of 1993P1 and an expiration date of 02/20. The package insert should be consulted for the usual adult dosage. The tablets should be stored at a controlled room temperature of 68-77F. The manufacturer of this drug is Lannett Company Inc. based in Philadelphia, PA. It is distributed by Redpharm Drug in Eden Prairie, MN.*

* 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.