Paroxetine Tablet, Film Coated
Product Images NDC 70518-3518

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Paroxetine (NDC 70518-3518). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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 paroxetine hydrochloride, depicting its molecular configuration with labeled fluorine and oxygen-containing groups, consistent with the active ingredient paroxetine.*

FDA Label Image

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A forest plot chart showing fold changes with 90% confidence intervals in pharmacokinetic parameters (Cmax and AUC) of several drugs interacting with Paroxetine. The x-axis represents change relative to reference values, featuring drugs Pimozide 2 mg, Desipramine 100 mg, Propranolol 80 mg twice daily, Digoxin 0.25 mg once daily, and Phenytoin 300 mg with corresponding fold change data points.*

FDA Label Image

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A forest plot showing fold change and 90% confidence intervals for pharmacokinetic parameters Cmax and AUC of Paroxetine when co-administered with various interacting drugs (Cimetidine, Phenobarbital, Phenytoin, Digoxin, Diazepam). The x-axis represents change relative to reference, illustrating the impact of each interacting drug on Paroxetine's pharmacokinetics.*

FDA Label Image

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A forest plot chart showing fold change and 90% confidence intervals for pharmacokinetic parameters (Cmax, Cmin, AUC) of Paroxetine in various populations, including renal impairment (mild, moderate, severe), hepatic impairment, age groups over 65 years with different dosages, and gender (males). The x-axis represents change relative to reference on a logarithmic scale from 0.5 to 50.*

FDA Label Image

Remedy_label (Remedy Label)

Paroxetine 20 mg tablet film coated label showing medication quantity of 100 tablets. The label indicates prescription use only, manufactured by Zydus Pharm, with repackaging by RemedyRepack Inc. The label states directions refer to the package insert, includes storage temperature guidance, and a warning to keep medication out of children's reach.*

* 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.