Hydrocodone Bitartrate And Acetaminophen Tablet
Product Images NDC 60760-692

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 60760-692). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by St. Mary's Medical Park Pharmacy, 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

60760-692 (Hydrocodone 60760 692 30)

Label for Hydrocodone Bitartrate and Acetaminophen tablets, USP 7.5 mg/325 mg, oral tablets. The label shows a 30-count package with NDC 60760-692-30, manufactured by Cranbury Pharmaceuticals, LLC, and packaged by St. Mary's Medical Park Pharmacy. It includes typical prescription labeling elements like lot number, expiration date placeholders, and storage instructions.*

FDA Label Image

Structure-1 (Hydrocodone Bitartrate And Acetaminophen Tablets 1)

Chemical structure diagram showing two molecular components, one with a complex ring structure including a methoxy group, and the other a smaller molecule with carboxyl and hydroxyl groups, along with notation indicating 2 1/2 water molecules (2.5 H2O). The image likely represents the chemical structures of hydrocodone bitartrate and an associated hydrate form.*

FDA Label Image

Structure-2 (Hydrocodone Bitartrate And Acetaminophen Tablets 2)

Chemical structure diagram of the active ingredient Hydrocodone Bitartrate and Acetaminophen showing the molecular arrangement including a benzene ring and functional groups.*

* 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.