Hydrocodone Bitartrate And Acetaminophen
Product Images NDC 42254-214

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Hydrocodone Bitartrate And Acetaminophen (NDC 42254-214). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rebel Distributors Corp, 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-structure (5f215257 7c82 478f A263 6fb37b438d69 01)

Chemical structure diagram illustrating the molecular composition of hydrocodone bitartrate with its corresponding bitartrate and water molecules (5/2 H2O), as indicated by the product data for hydrocodone bitartrate and acetaminophen from Rebel Distributors Corp.*

FDA Label Image

Acetaminophen-structure (5f215257 7c82 478f A263 6fb37b438d69 02)

Chemical structure diagram showing the molecular structure of the active ingredient, likely acetaminophen, as part of HYDROCODONE BITARTRATE AND ACETAMINOPHEN. The diagram includes aromatic ring, hydroxyl group, amide linkage, and carbonyl group elements.*

FDA Label Image

Dea (5f215257 7c82 478f A263 6fb37b438d69 03)

FDA Label Image

Hydrocodone 10mg/acet 325mg (5f215257 7c82 478f A263 6fb37b438d69 04)

Label for Hydrocodone 10mg and Acetaminophen 325mg oral tablets by Rebel Distributors Corp under the Physician Partner brand, with NDC 42254-214-90. The label states it contains 90 tablets and describes the tablets as white to off-white, oval, biconvex, and uncoated, debossed with '176' and scored. Manufactured by Sun Pharmaceutical Industries, Inc., Cranbury, NJ. Storage instructions and safety warnings are included.*

* 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.