Butalbital, Acetaminophen And Caffeine Tablet
Product Images NDC 71335-2546

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 71335-2546). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

Chemsture-butalbital (Chemsture)

Chemsture-butalbital (Chemsture)
Chemical structure diagram showing a molecular formula with labeled atoms and bonds, representing the chemical structure of the active ingredient in the product Butalbital, Acetaminophen, and Caffeine.*
FDA Label Image

Chemsture-acetaminophen (Chemsture00)

Chemsture-acetaminophen (Chemsture00)
Chemical structure of acetaminophen, showing a benzene ring with hydroxyl (OH) and acetamido (NHCOCH3) functional groups.*
FDA Label Image

Chemsture-ceffeine (Chemsture01)

Chemsture-ceffeine (Chemsture01)
Chemical structure diagram of the active ingredient caffeine, showing its molecular formula C8H10N4O2 and molecular weight 194.19.*
FDA Label Image

Label (Lbl713352546)

Label (Lbl713352546)
Label for Butalbital, Acetaminophen and Caffeine Tablets, USP with strengths 50 mg, 325 mg, and 40 mg respectively. The label includes NDC 71335-2546-1, states the product is prescription-only, and indicates a package size of 20 tablets. It is repackaged by Bryant Ranch Prepack and manufactured by Quagen Pharmaceuticals LLC. Storage and dosage information are also provided along with QR codes for package inserts.*

* 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.