Hydrocodone Bitartrate And Acetaminophen
Product Images NDC 50090-1518

3 FDA label images from A-s Medication Solutions · 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 50090-1518). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by A-s Medication Solutions, 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

This Is An Image Of The Structural Formula Of Hydrocodone Bitartrate. (Hydro 1)

This Is An Image Of The Structural Formula Of Hydrocodone Bitartrate. (Hydro 1)
Chemical structure diagram of Hydrocodone Bitartrate and Acetaminophen showing molecular components and hydrated water molecules with molecular weight of 494.5.*
FDA Label Image

This Is An Image Of The Structural Formula Of Acetaminophen. (Hydro 2)

This Is An Image Of The Structural Formula Of Acetaminophen. (Hydro 2)
Chemical structure diagram showing the molecular structure of an unidentified compound including chemical groups such as CH3CONH and OH. Molecular weight is indicated as 151.16. The image appears to be a partial chemical structure likely related to an active ingredient.*
FDA Label Image

Label Image (Lbl500901518)

Label Image (Lbl500901518)
Label for Hydrocodone Bitartrate And Acetaminophen 5 mg / 325 mg tablets, containing 20 tablets. The label includes the NDC 50090-1518-0 and denotes the product as prescription only (Rx Only). It is labeled by A-S Medication Solutions LLC with storage instructions and warnings about drug transfer and child safety.*

* 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.