Tramadol Hydrochloride
Product Images NDC 64205-627

4 FDA label images from Readymeds · 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 64205-627). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Readymeds, 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

7bb9a2e6-figure-01 (7bb9a2e6 Figure 01)

7bb9a2e6-figure-01 (7bb9a2e6 Figure 01)
Chemical structure of Tramadol Hydrochloride showing its molecular bonds and functional groups, including a cyclohexane ring, hydroxyl group, methoxybenzene, and amine moiety with hydrochloride salt representation.*
FDA Label Image

7bb9a2e6-figure-02 (7bb9a2e6 Figure 02)

7bb9a2e6-figure-02 (7bb9a2e6 Figure 02)
A pharmacokinetic curve showing plasma concentration (ng/mL) over time (hours) for Tramadol and its metabolite M1. The graph compares multiple-dose and single-dose profiles, with separate lines for Tramadol and M1 concentrations over a 48-hour period.*
FDA Label Image

7bb9a2e6-figure-03 (7bb9a2e6 Figure 03)

7bb9a2e6-figure-03 (7bb9a2e6 Figure 03)
A step plot chart titled 'Protocol CAPSS-047 Time to Discontinuation Due to Nausea/Vomiting' showing percent discontinuing over days in a double-blind study, with a label indicating '10 days to 200 mg/day.' The y-axis ranges from 0 to 50 percent discontinuing, and the x-axis measures days up to 25.*
FDA Label Image

Image Description (Photo)

Image Description (Photo)
Label for ReadyMeds Tramadol Hydrochloride 50 mg, bottle of 30 tablets. The label displays the NDC number 64205-627-30, expiration date 11/2016, and lot number HL20613A.*

* 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.