Escitalopram Oxalate Tablet, Film Coated
Product Images NDC 68645-520

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Escitalopram Oxalate (NDC 68645-520). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Legacy Pharmaceutical Packaging, Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

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6.1 Clinical Trials Experience (Table 2)

A data table comparing adverse reactions between escitalopram (N=715) and placebo (N=592) groups. It lists percentages of participants experiencing various side effects categorized by system disorders such as autonomic nervous system, central and peripheral nervous system, gastrointestinal, general, psychiatric, respiratory, and urogenital disorders. The table shows higher incidence rates of most side effects in the escitalopram group compared to placebo.*

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Clinical Trials Experience (Table3)

Table showing adverse reactions observed with a frequency of 2% or more and placebo comparison for Escitalopram versus placebo in adults with Generalized Anxiety Disorder. Categories include autonomic nervous system disorders, central and peripheral nervous system disorders, gastrointestinal disorders, general, musculoskeletal system disorder, psychiatric disorders, respiratory system disorders, and urogenital. Percentages for each adverse reaction are given for Escitalopram (N=429) and placebo (N=427) groups.*

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Image (Escitalopram Tabs Cipla Bottle 4)

A data table presenting the incidence of common adverse reactions in patients with major depressive disorder treated with Escitalopram Oxalate at daily doses of 10 mg and 20 mg compared to placebo. The table lists various adverse reactions and their percentages across placebo and two Escitalopram dose groups.*

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Image (Escitalopram Tabs Cipla Bottle 5)

A data table titled 'Incidence of Sexual Side Effects in Placebo-Controlled Clinical Trials' comparing the percentage of adverse events for Escitalopram versus placebo. The table is divided by gender, reporting specific issues such as ejaculation disorder, decreased libido, impotence in males, and decreased libido and anorgasmia in females.*

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7 Drug Interactions (Table 6)

A detailed drug interaction and clinical impact table for Escitalopram Oxalate. It covers interactions with monoamine oxidase inhibitors (MAOIs), pimozide, serotoninergic drugs, NSAIDs and anticoagulants, sumatriptan, carbamazepine, and CYP2D6-metabolized drugs. Each section includes clinical impacts and intervention recommendations associated with Escitalopram Oxalate use.*

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Image (Escitalopram Tabs Cipla Bottle 6)

Chemical structure of Escitalopram Oxalate shown as a molecular diagram with labeled atoms and bonds, including the oxalate component (C2H2O4).*

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Package Label Principal Display Panel (Escitalopram 10mg)

Escitalopram Tablets, USP 10 mg tablet label showing the product name, strength, and dosage form. The label indicates 30 tablets per package and includes a blue and purple design highlight. It states the product is Rx Only and provides storage instructions, dispensing guidance, and warnings. Manufactured for Cipla USA Inc. and packaged by Legacy Pharmaceutical Packaging LLC, Earth City, MO.*

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Package Label Principal Display Panel (Escitalopram 20mg)

Escitalopram Tablets USP 20 mg tablet label from Legacy Pharmaceutical Packaging, LLC. The label states 20 mg strength and quantity of 30 tablets. It includes usage instructions, storage conditions, warnings, and distribution information. The packaging indicates prescription use only and features a tablet image imprinted with 'IG' and '25I'.*

* 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.