Butalbital And Acetaminophen
Product Images NDC 0722-7075

3 FDA label images from Nexgen Pharma, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Butalbital And Acetaminophen (NDC 0722-7075). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nexgen Pharma, 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

Butalbital Molecule (E93a6fd5 Ef69 4bb9 Bfd8 390c5f35884c 01)

Butalbital Molecule (E93a6fd5 Ef69 4bb9 Bfd8 390c5f35884c 01)
Chemical structure of the active ingredient in Butalbital and Acetaminophen. The diagram shows a molecular structure including carbon, hydrogen, nitrogen, and oxygen atoms arranged in a bicyclic ring system with side chains.*
FDA Label Image

Apap Molecule (E93a6fd5 Ef69 4bb9 Bfd8 390c5f35884c 02)

Apap Molecule (E93a6fd5 Ef69 4bb9 Bfd8 390c5f35884c 02)
Chemical structure of Acetaminophen showing a benzene ring with hydroxyl and amide groups attached.*
FDA Label Image

Ba 300 Serialized Container Label (E93a6fd5 Ef69 4bb9 Bfd8 390c5f35884c 03)

Ba 300 Serialized Container Label (E93a6fd5 Ef69 4bb9 Bfd8 390c5f35884c 03)
Label for Butalbital and Acetaminophen tablets, 50 mg/300 mg strength, from Nexgen Pharma, Inc. The label shows the quantity of 100 tablets and includes dosage information advising 1 or 2 tablets every four hours with a daily maximum of 6 tablets. It contains warnings about habit-forming properties and storage instructions to keep the medication out of reach of children and store at 20 to 25°C. Manufacturer details and a barcode are visible.*

* 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.