Citalopram Hydrobromide Tablet, Film Coated
Product Images NDC 80425-0309

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Citalopram Hydrobromide (NDC 80425-0309). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Advanced Rx Pharmacy Of Tennessee, 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.

FDA Label Image

Label 1 (Citalopram Hydrobromide 10mg 80425 0309 01)

Citalopram Hydrobromide 10 mg tablet packaging label from Advanced Rx Pharmacy of Tennessee, LLC, Nashville TN. The label includes the NDC 80425-0309 and states comparison to Celexa. It shows a 30 count, storage instructions at 20-25°C, and an expiration date of 8/31/2025.*

FDA Label Image

Label 2 (Citalopram Hydrobromide 10mg 80425 0309 02)

Label for Citalopram Hydrobromide 10 mg film-coated tablets by Advanced Rx Pharmacy of Tennessee, LLC. The label states storage conditions (20°-25°C), contains a caution to read the label for PROBIMS transfer warning, compares the product to CELEXA, and displays the NDC number 80425-0309 along with lot and expiration date fields. The package quantity is #60 tablets.*

FDA Label Image

Label 3 (Citalopram Hydrobromide 10mg 80425 0309 03)

Citalopram Hydrobromide 10 mg film-coated tablet label from Advanced Rx Pharmacy of Tennessee, LLC. The label includes storage instructions (20-25°C), a barcode, lot number, expiration date (8/31/2025), and a comparison to Celexa. The product NDC is 80425-0309-03.*

FDA Label Image

Description (Description)

Chemical structure diagram of Citalopram Hydrobromide, the active ingredient in the product Citalopram Hydrobromide 10 mg film-coated tablets from Advanced Rx Pharmacy of Tennessee, LLC.*

* 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.