Tramadol Hydrochloride Tablet
Product Images NDC 71335-2518

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Tramadol Hydrochloride (NDC 71335-2518). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

Label (Lbl713352518)

Label (Lbl713352518)
This text provides important information about Tramadol Hydrochloride tablets, USP, with each tablet containing 50 mg of the active ingredient. The recommended dosage instructions direct pharmacists to dispense a Medication Guide to each patient and store the tablets in a tight, light-resistant container at room temperature. The NDC code for the product is 71335-2518-1, and it is indicated for prescription use only. The tablets are repackaged by Bryant Ranch Prepack, Inc. and manufactured by Elysium Pharmaceuticals, based in Burbank, CA, USA. Pharmacists are advised to refer to the package insert for complete product information.*
FDA Label Image

Figure 1 (Tramadol 02)

FDA Label Image

Figure 2 (Tramadol 03)

Figure 2 (Tramadol 03)
This chart shows the percentage of participants discontinuing a protocol (CAPSS-047) over time due to nausea and vomiting. The data is displayed for days 0 to 25 in a double-blind study. This information can be useful for analyzing the impact of these symptoms on the study participants' ability to continue with the protocol.*
FDA Label Image

Structure (Tramadol 1)

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