Butalbital, Acetaminophen And Caffeine
Product Images NDC 68387-520

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Butalbital, Acetaminophen And Caffeine (NDC 68387-520). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Keltman 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

Label Image (Fioricet Tablet Lab)

Label Image (Fioricet Tablet Lab)
Label for Butalbital 50mg, Acetaminophen (APAP) 325mg, and Caffeine 40mg tablets by Keltman Pharmaceuticals Inc. The label indicates 30 tablets per bottle, marked Rx Only. It includes lot number 64540A1, expiration date 11/2011, and prescription number 152920. Manufactured by West-ward Pharmaceutical Corp and distributed by Keltman Pharmaceuticals.*
FDA Label Image

Figure 1 (Bact 01)

Figure 1 (Bact 01)
Chemical structure diagram showing the molecular formula and structure of Butalbital, Acetaminophen, and Caffeine combined, including atomic connections and molecular weight details.*
FDA Label Image

Figure 2 (Bact 02)

Figure 2 (Bact 02)
Chemical structure of Butalbital, Acetaminophen and Caffeine active ingredients, showing the molecular arrangement including hydroxyl, acetamido, and other functional groups with a molecular weight of 151.17.*
FDA Label Image

Figure 3 (Bact 03)

Figure 3 (Bact 03)
Chemical structure of the active ingredient, Caffeine, as indicated by the molecular formula and weight provided. The structure shows the arrangement of atoms and bonds characteristic of caffeine.*

* 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.