Escitalopram Oxalate
Product Images NDC 68071-3312

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Escitalopram Oxalate (NDC 68071-3312). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nucare 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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A data table titled 'Treatment-Emergent Adverse Reactions observed with a frequency of ≥ 2% and greater than placebo for Major Depressive Disorder.' It compares adverse reactions between escitalopram oxalate (N=715) and placebo (N=592) groups, listing various disorder categories and specific symptoms with percentage incidences for each treatment.*

FDA Label Image

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Table presenting treatment-emergent adverse reactions with escitalopram oxalate compared to placebo for Generalized Anxiety Disorder, showing reaction frequencies greater than 2%, categorized by system disorders such as autonomic nervous, central & peripheral nervous, gastrointestinal, general, musculoskeletal, psychiatric, respiratory, and urogenital systems.*

FDA Label Image

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Chemical structure of escitalopram oxalate, depicting its molecular configuration with marked functional groups and the oxalate component shown as C2H2O4.*

FDA Label Image

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FDA Label Image

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FDA Label Image

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Label for escitalopram oxalate 20 mg tablets by NuCare Pharmaceuticals, Inc. The label indicates a package of 30 film-coated tablets. Details include lot number, expiration date, and NDC 68071-3312-3. Tablets are described as round, white/off-white, scored, with specific debossing marks. The label also advises to take every 12 hours and includes storage instructions at controlled temperature 59-86°F.*

* 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.