Tramadol Hydrochloride
Product Images NDC 45865-900

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Tramadol Hydrochloride (NDC 45865-900). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Medsource Pharmaceuticals, 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

Pdp (900)

This is a description of a medication called Tramadol HCL ER, which is available in the form of tablets with a strength of 200mg. It is a generic version of a medication called LLTRAM ER and the product code is 45865050030. The medication is available in a package of 30 tablets with the name SINBRARI D on it. The dosage and usage details are not available in the given text.*

FDA Label Image

Tramadol-figure1 (Tramadol Figure1)

Hydrochloride is a medication available in two forms, extended-release tablets and immediate-release tablets. The extended-release tablets are taken once a day in a 200mg dose, while the immediate-release tablets are taken every six hours in a 50mg dose. This text appears to be a medication label or prescription instructions.*

FDA Label Image

Tramadol-figure2 (Tramadol Figure2)

The text describes two types of tablets: Tramadol Hydrochloride Extended-Release Tablets with a dosage of 200 mg to be taken once a day, and Tramadol IR Tablets with a dosage of 50 mg to be taken every six hours. There is also a code or label "W1 Gonsersration (ne/mt)" and another code or label "M1".*

FDA Label Image

Tramadol-figure3 (Tramadol Figure3)

FDA Label Image

Tramadol-figure4 (Tramadol Figure4)

FDA Label Image

Tramadol-structure (Tramadol Structure)

* 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.