Hydrocodone Bitartrate And Acetaminophen Tablet
Product Images NDC 63629-2309

3 FDA label images from Bryant Ranch Prepack · 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 63629-2309). 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

Hydrocodone Bitartrate Structural Formula (Hydrocodone Bitartrate And Acetaminophen Tablets 1)

Hydrocodone Bitartrate Structural Formula (Hydrocodone Bitartrate And Acetaminophen Tablets 1)
Chemical structure diagram showing molecular components associated with Hydrocodone Bitartrate and Acetaminophen. The illustration includes structural formulas of organic molecules with carbon, hydrogen, oxygen, and nitrogen atoms typical for these active ingredients.*
FDA Label Image

Acetaminophen Structural Formula (Hydrocodone Bitartrate And Acetaminophen Tablets 2)

Acetaminophen Structural Formula (Hydrocodone Bitartrate And Acetaminophen Tablets 2)
Chemical structure diagram depicting the molecular structure of acetaminophen, showing the arrangement of hydroxyl, amide, and aromatic functional groups characteristic of the compound.*
FDA Label Image

Label (Lbl636292309)

Label (Lbl636292309)
Label for Hydrocodone Bitartrate and Acetaminophen Tablets, USP, 7.5 mg/300 mg, oral tablets. The label shows the NDC 63629-2309-1, manufacturer Tirs Pharma, Inc., and labeler Bryant Ranch Prepack. Package contains 100 tablets, marked Rx only. The label includes storage instructions and a caution about overdose risk.*

* 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.