Hydrocodone Bitartrate And Acetaminophen
Product Images NDC 64725-0026

3 FDA label images from Tya Pharmaceuticals · 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 Hydrocodone Bitartrate And Acetaminophen (NDC 64725-0026). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Tya Pharmaceuticals, 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 (64725 0026)

Label Image (64725 0026)
Label for HYDROCODONE BITARTRATE AND ACETAMINOPHEN 5 mg / 325 mg tablets, with 30 tablets per container. The label includes prescription status, lot number placeholder, expiration date placeholder, and manufacturer listed as SUN PHARMA. It also notes repackaging by TYA Pharmaceuticals with a Tallahassee, FL address and contact phone. Barcode and dose instruction to see package insert are visible.*
FDA Label Image

Hydrocodone-structure (Hydrocodone Structure)

Hydrocodone-structure (Hydrocodone Structure)
Chemical structure diagram of hydrocodone bitartrate and acetaminophen, showing their molecular compositions including functional groups and stereochemistry.*
FDA Label Image

Acetaminophen-structure (Hydrocodone Structure1)

Acetaminophen-structure (Hydrocodone Structure1)
Chemical structure of acetaminophen, one of the active ingredients in HYDROCODONE BITARTRATE AND ACETAMINOPHEN by TYA Pharmaceuticals. The structure shows a benzene ring with a hydroxyl group (OH) and an amide group (NH-CO-CH3) attached.*

* 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.