Paroxetine Tablet, Film Coated
Product Images NDC 68382-098

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Paroxetine (NDC 68382-098). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zydus 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 Paroxetine hydrochloride illustrating its molecular framework with fluorophenyl, piperidine, and dioxolane components as represented in the diagram.*

FDA Label Image

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A forest plot chart showing fold changes and 90% confidence intervals for pharmacokinetic parameters (Cmax and AUC) of various interacting drugs, including Pimozide 2 mg, Desipramine 100 mg, Propranolol 80 mg twice daily, Digoxin 0.25 mg once daily, and Phenytoin 300 mg, relative to reference values.*

FDA Label Image

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A forest plot chart showing the pharmacokinetic interactions of Paroxetine with various drugs. It displays fold change and 90% confidence intervals for Cmax and AUC values relative to reference for drugs including Cimetidine, Phenobarbital, Phenytoin, Digoxin, and Diazepam, indicating their effect on Paroxetine's pharmacokinetics.*

FDA Label Image

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

FDA Label Image

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Paroxetine Tablets, USP 10 mg film-coated oral tablets label by Zydus Pharmaceuticals USA Inc. The label indicates a package of 500 tablets and includes dosage strength, NDC 68382-097-05, barcode, and manufacturer details. It features usage instructions, storage conditions, and a reminder to dispense the Medication Guide separately to each patient.*

FDA Label Image

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Paroxetine Tablets, USP 20 mg film-coated tablets in a package labeled for 1,000 tablets. The label includes dosage strength, NDC 68382-098-10, and states the product is prescription only. It is distributed by Zydus Pharmaceuticals USA Inc. The label instructs pharmacists to dispense a separate Medication Guide and provides storage and safety instructions.*

FDA Label Image

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Paroxetine Tablets, USP 30 mg film-coated tablets label for oral use, manufactured by Zydus Pharmaceuticals USA Inc. The label states the package contains 1,000 tablets and includes dosage and storage instructions, safety warnings, and distributor information. The NDC code 68382-099-10 is shown on the label along with the Zydus Pharmaceuticals logo.*

FDA Label Image

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Paroxetine Tablets USP 40 mg film-coated tablets label by Zydus Pharmaceuticals USA Inc. The label indicates a package of 30 tablets with NDC 68382-001-06 and includes usage and storage information, a pharmacist dispensing instruction, and manufacturer details. The label features a barcode and warnings about child-resistance and safety closures.*

* 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.