Imatinib Mesylate Tablet, Film Coated
Product Images NDC 0093-7630

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Imatinib Mesylate (NDC 0093-7630). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Teva Pharmaceuticals Usa, 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 Imatinib Mesylate, showing its molecular components and arrangement including aromatic rings, nitrogen atoms, and a mesylate group.*

FDA Label Image

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A Kaplan-Meier survival curve graph showing percentage without progression over months since randomization. It compares two treatment arms for Imatinib Mesylate and IFN+Ara-C, illustrating patient progression data, hazard ratio, confidence interval, and log-rank test significance.*

FDA Label Image

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A Kaplan-Meier survival curve comparing Imatinib Mesylate and IFN+Ara-C arms, showing the percentage of patients without progression to AP/BC over months since randomization. The graph includes patient numbers, hazard ratio with confidence interval, and statistical significance (P < 0.001).*

FDA Label Image

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Label for Imatinib Mesylate 100 mg film-coated tablets by Teva Pharmaceuticals USA, Inc. The label indicates it is a prescription drug containing 90 tablets. Storage instructions and lot/expiration date sections are also shown. The NDC is 0093-7629-98.*

FDA Label Image

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Label for Imatinib Mesylate 400 mg film-coated tablets by Teva Pharmaceuticals USA, Inc. The label indicates a package of 30 tablets for oral use, with NDC 0093-7630-56. The label includes storage instructions and a lot/expiration date area.*

* 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.