Hydrocodone Bitartrate And Acetaminophen Tablet
Product Images NDC 63629-2310

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 63629-2310). 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 depicting the active ingredients hydrocodone bitartrate and acetaminophen in the Hydrocodone Bitartrate and Acetaminophen oral tablet product by Bryant Ranch Prepack.*
FDA Label Image

Acetaminophen Structural Formula (Hydrocodone Bitartrate And Acetaminophen Tablets 2)

Acetaminophen Structural Formula (Hydrocodone Bitartrate And Acetaminophen Tablets 2)
Chemical structure of acetaminophen (paracetamol), showing a benzene ring with hydroxyl and amide functional groups.*
FDA Label Image

Label (Lbl636292310)

Label (Lbl636292310)
Label for Hydrocodone Bitartrate and Acetaminophen Tablets, USP, with strength 10 mg/300 mg. The label displays the NDC 63629-2310-1, indicates it is for prescription use only, and contains 100 tablets. The product is labeled by Bryant Ranch Prepack and manufactured by Tris Pharma, Inc. The label includes storage instructions, a child-resistant container warning, and a caution about overdose and addiction 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.