Citalopram
Product Images NDC 10544-182

3 FDA label images from Blenheim Pharmacal, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Citalopram (NDC 10544-182). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Blenheim Pharmacal, 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

Label 20mg 30ct (Label Citalopram Tabs 20mg Bpi(10544 179 30) Epic(42806 020 10) Rev2)

Label 20mg 30ct (Label Citalopram Tabs 20mg Bpi(10544 179 30) Epic(42806 020 10) Rev2)
Label for Citalopram Tablets, USP 20 mg, containing 30 tablets. It is produced by Blenheim Pharmacal, Inc. The label includes storage instructions for controlled room temperature and a warning to keep out of reach of children. The NDC number 10544-179-30 and manufacturer code 42806-020-10 are also present.*
FDA Label Image

Label 40mg 30ct (Label Citalopram Tabs 40mg Bpi(10544 182 30) Epic(42806 021 10) Rev1)

Label 40mg 30ct (Label Citalopram Tabs 40mg Bpi(10544 182 30) Epic(42806 021 10) Rev1)
Citalopram Tablets USP 40mg bottle label by Blenheim Pharmacal, Inc., showing a 30 tablet count. The label includes storage instructions, dosage note, and barcode. It specifies that the product is prescription only and provides NDC and manufacturer numbers.*
FDA Label Image

Structure (Image 01)

Structure (Image 01)
Chemical structure diagram of the active ingredient Citalopram, showing its molecular composition including aromatic rings, fluorine, and other functional groups. The image also shows the hydrobromide salt form (.HBr).*

* 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.