Tramadol Hydrochloride Tablet, Extended Release
Product Images NDC 68180-698

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Tramadol Hydrochloride (NDC 68180-698). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lupin Pharmaceuticals, 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

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Chemical structure of Tramadol Hydrochloride, showing the molecular arrangement including a cyclohexane ring, methoxyphenyl group, and dimethylaminomethyl side chain with associated hydrochloride.*

FDA Label Image

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A line graph comparing Tramadol concentration (ng/mL) over 24 hours for two formulations: Tramadol Hydrochloride Extended-Release Tablets 200 mg once daily and Tramadol Hydrochloride Tablets 50 mg every 6 hours. The graph shows time (hours) on the x-axis and Tramadol concentration on the y-axis, with distinct markers for each formulation over time.*

FDA Label Image

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A concentration-time line graph comparing M1 metabolite levels in ng/mL over 24 hours following oral administration of Tramadol Hydrochloride Extended-Release Tablets 200 mg once daily versus Tramadol Hydrochloride Tablets 50 mg every 6 hours. The x-axis represents time in hours, and the y-axis represents M1 concentration in ng/mL, showing pharmacokinetic profiles of both dosage forms.*

FDA Label Image

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A line graph titled 'Tramadol Hydrochloride Extended-Release Tablets Study 023 WOMAC Pain Responder Analysis.' It shows the percent of patients achieving various levels of response thresholds in percent improvement from baseline for Tramadol Hydrochloride extended-release tablets at 100 mg, 200 mg, 300 mg, 400 mg doses, and placebo. The x-axis represents the response threshold in percent improvement, and the y-axis shows the percent of patients achieving response, with multiple lines comparing each dosage and placebo outcomes.*

FDA Label Image

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A line graph titled "Tramadol Hydrochloride Extended-Release Tablets Study 015 Arthritis Pain Intensity VAS Responder Analysis" showing percent of patients achieving various levels of response threshold. The x-axis represents response threshold as percent improvement from baseline, ranging from 0 to 100. The y-axis shows the percent of patients achieving response, from 0 to 60%. Two lines compare Tramadol Hydrochloride extended-release tablets (marked with open circles) and placebo (marked with stars), demonstrating higher patient response percentages with Tramadol Hydrochloride across all thresholds.*

FDA Label Image

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Label for Tramadol Hydrochloride Extended-release Tablets USP 100 mg by Lupin Pharmaceuticals, Inc. The label indicates a 30-tablet package with instructions for once-daily use. It includes NDC 68180-697-06, storage guidelines, barcode, QR code for medication guide, and manufacturer information in Baltimore, Maryland.*

FDA Label Image

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Label for Tramadol Hydrochloride Extended-release Tablets USP, 200 mg strength, manufactured by Lupin Pharmaceuticals, Inc. The label indicates 30 tablets per package and includes dosing, storage, and warning information along with a barcode and QR code for medication guide access. The product is for oral use and prescription only.*

FDA Label Image

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Label for Tramadol Hydrochloride Extended-release Tablets USP 300 mg, oral extended-release tablets. The label states once daily use, contains 30 tablets, and is manufactured by Lupin Pharmaceuticals, Inc. It includes storage instructions, a barcode, and a QR code linking to a medication guide. The label prominently displays the strength and drug name.*

* 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.