Hydrocodone Bitartrate And Acetaminophen Tablet
Product Images NDC 82804-116

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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 82804-116). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Proficient Rx Lp, 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

Chemical Structure Of Hydrocodone Bitartrate (Hydrocodone Bitartrate And Acetaminophen Tablet 1)

Chemical Structure Of Hydrocodone Bitartrate (Hydrocodone Bitartrate And Acetaminophen Tablet 1)
Chemical structure of hydrocodone bitartrate showing the molecular formulas and associated water of hydration with a molecular weight of 494.490.*
FDA Label Image

Chemical Structure Of Acetaminophen (Hydrocodone Bitartrate And Acetaminophen Tablet 2)

Chemical Structure Of Acetaminophen (Hydrocodone Bitartrate And Acetaminophen Tablet 2)
Chemical structure of acetaminophen showing its molecular formula C8H9NO2 and molecular weight 151.16.*
FDA Label Image

82804-116-12 (Hydrocodone Bitartrate And Acetaminophen Tablet 3)

82804-116-12 (Hydrocodone Bitartrate And Acetaminophen Tablet 3)
Label for Hydrocodone / APAP 5mg/325mg tablets, containing 12 tablets. The label states each tablet contains Hydrocodone Bitartrate 5 mg and Acetaminophen 325 mg. It includes dosage form as capsule-shaped white tablets debossed with M365 on one side, bisected on the other. The product is labeled Rx Only, Schedule C-II, and manufactured by SpecGx LLC, Webster Groves, MO. Storage instructions and multiple NDC codes appear, with a barcode and Proficient Rx logo.*

* 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.