Citalopram Hydrobromide Tablet
Product Images NDC 50090-3208

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Citalopram Hydrobromide (NDC 50090-3208). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by A-s Medication Solutions, 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 Citalopram Hydrobromide active ingredient, showing its molecular arrangement including aromatic rings, fluorine atom, nitrogen-containing side chain, and hydrobromide component.*

FDA Label Image

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FDA Label Image

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FDA Label Image

Label Image (Lbl500900892)

Label for Citalopram Hydrobromide 20 mg tablets by A-S Medication Solutions. The label specifies 30 tablets per package, storage instructions to keep at 68 to 77 degrees Fahrenheit, and includes a National Drug Code (NDC) 50090-0892-0. The product number 5626-0 is also shown with dosage and packaging information.*

FDA Label Image

Label Image (Lbl500901298)

Citalopram Hydrobromide 10 mg tablet bottle label from A-S Medication Solutions. The label indicates each tablet contains 10 mg of citalopram hydrobromide, USP, equivalent to 10 mg citalopram. The bottle contains 100 tablets and storage instructions specify 68 to 77 degrees Fahrenheit. The label also includes the product number 6322-0 and NDC 50090-1298-0.*

FDA Label Image

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The label for Citalopram Hydrobromide 40 mg tablets by A-S Medication Solutions displays product number 5627-0 and NDC 50090-3208-0. It states that each tablet contains citalopram hydrobromide equivalent to 40 mg citalopram. The label advises storage at 68 to 77 degrees Fahrenheit and indicates the package contains 30 tablets.*

* 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.