Butalbital, Acetaminophen, Caffeine Tablet
Product Images NDC 68788-8137

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Butalbital, Acetaminophen, Caffeine (NDC 68788-8137). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Preferred Pharmaceuticals 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

Chemical Structure (Butalbital 01)

Chemical structure diagram of the active ingredient acetaminophen, depicting its molecular framework with atoms and bonds. The structure shows the arrangement of carbon, hydrogen, nitrogen, and oxygen atoms characteristic of acetaminophen.*

FDA Label Image

Chemical Structure (Butalbital 02)

Chemical structure diagram of acetaminophen, displaying the arrangement of atoms and bonds characteristic of this active ingredient in the medication Butalbital, Acetaminophen, and Caffeine tablets by Preferred Pharmaceuticals Inc.*

FDA Label Image

Chemical Structure (Butalbital 03)

Chemical structure diagram of the active ingredient caffeine, showing its molecular formula and arrangement of atoms in a two-ring fused structure with methyl and nitrogen groups.*

FDA Label Image

Butalbital Acet And Caffeine Tab 50/325/40mg Ciii (Butalbital 04)

Label for Butalbital, Acetaminophen, and Caffeine tablets, strength 50 mg / 325 mg / 40 mg, classified as CIII. The label states it is a generic for Fioricet, manufactured by Westminster Pharmaceuticals, LLC. Instructions are provided in English and Spanish for dosage frequency. The label includes storage information, warnings, barcode, and the Preferred Pharmaceuticals logo.*

* 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.