Butalbital, Acetaminophen And Caffeine Tablet
Product Images NDC 51407-556

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 51407-556). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Golden State Medical Supply, 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

51407-556-01lb.jpg (51407 556 01lb)

51407-556-01lb.jpg (51407 556 01lb)
Label for Butalbital, Acetaminophen and Caffeine tablets, USP, containing 50 mg Butalbital, 325 mg Acetaminophen, and 40 mg Caffeine per tablet. The label shows a quantity of 100 tablets and is marked Rx Only. Manufactured by Granules Pharmaceuticals Inc. and marketed by GSMS, Incorporated. NDC 51407-556-01.*
FDA Label Image

Fig-1 (Figure 1)

Fig-1 (Figure 1)
Chemical structure diagram showing the molecular structure of the active ingredient in Butalbital, Acetaminophen and Caffeine tablets. The structure features a hexagonal ring with various chemical groups attached, corresponding to the butalbital component.*
FDA Label Image

Fig-2 (Figure 2)

Fig-2 (Figure 2)
Chemical structure diagram showing a substituted benzene ring with hydroxyl (OH) and acetamido (NHCOCH3) functional groups. This image likely represents the chemical structure of acetaminophen, one of the active ingredients in Butalbital, Acetaminophen and Caffeine tablets.*
FDA Label Image

Fig-3 (Figure 3)

Fig-3 (Figure 3)
Chemical structure diagram of the active ingredient caffeine. The image shows a molecular formula with labeled atoms and bonds representing caffeine's chemical configuration.*

* 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.