Escitalopram Tablet, Film Coated
Product Images NDC 16571-756

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Escitalopram (NDC 16571-756). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rising Pharma Holdings, 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 escitalopram, showing its molecular framework including aromatic rings, nitrogen, oxygen, fluorine, and an attached ethyl group. The structure also includes the formula for an associated oxalate moiety (C2H2O4).*

FDA Label Image

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Label for Escitalopram Tablets USP 5 mg, film-coated tablets in a 100-count package by Rising Pharma Holdings, Inc. Instruction for pharmacists to dispense the Medication Guide separately is included. The label states storage conditions, dosage reference, and manufacturer details for Graviti Pharmaceuticals Pvt. Ltd., India.*

FDA Label Image

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Label for Escitalopram Tablets, USP 10 mg, film-coated tablets for oral use. The label shows the product is supplied by Rising Pharma Holdings, Inc., with 100 tablets per container. It notes each tablet contains escitalopram oxalate equivalent to 10 mg escitalopram and storage instructions. The label includes distributor and manufacturer details, barcode, and mentions the product is Rx only.*

FDA Label Image

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Label for escitalopram tablets, USP 20 mg oral film-coated tablets by Rising Pharma Holdings, Inc. The package contains 100 tablets. The label includes storage instructions, dispensing guidance, manufacturer and distributor information, and a note about an available Medication Guide.*

* 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.