Hydrocodone Bitartrate And Acetaminophen Tablet
Product Images NDC 60760-873

View Photos of 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 60760-873). 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

873-60 (Hydrocodone 60760 873 60)

873-60 (Hydrocodone 60760 873 60)
Label for Hydrocodone Bitartrate and Acetaminophen tablets USP, 5 mg/325 mg strength, in a quantity of 60. The label includes NDC 60760-873-60, manufacturer Cranbury Pharmaceuticals, LLC, and packager St. Mary's Medical Park Pharmacy. It displays lot, expiration, and prescription numbers as placeholders, with storage instructions at controlled room temperature (15°-30°C). The label also features a barcode and a QR code.*
FDA Label Image

Structure-1 (Hydrocodone Bitartrate And Acetaminophen Tablets 1)

Structure-1 (Hydrocodone Bitartrate And Acetaminophen Tablets 1)
Chemical structure diagram showing two molecular structures side by side, representing the active ingredients hydrocodone bitartrate and acetaminophen components, with detailed bonds and atoms including oxygen and hydrogen groups visible.*
FDA Label Image

Structure-2 (Hydrocodone Bitartrate And Acetaminophen Tablets 2)

Structure-2 (Hydrocodone Bitartrate And Acetaminophen Tablets 2)
Chemical structure diagram of Hydrocodone Bitartrate and Acetaminophen showing the molecular arrangement with a phenol (HO attached to a benzene ring), amide linkage, and acetyl group consistent with acetaminophen.*

* 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.