Oxycodone And Acetaminophen
Product Images NDC 72022-584

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Oxycodone And Acetaminophen (NDC 72022-584). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Halo Pharmaceutical Inc, 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

10 mg/325 mg 100 Tablets (10mg 325mg Tabs 100 Nj)

10 mg/325 mg 100 Tablets (10mg 325mg Tabs 100 Nj)
Label for Oxycodone and Acetaminophen Tablets, USP 10 mg / 325 mg by Halo Pharmaceutical Inc. The label lists each tablet containing 10 mg Oxycodone Hydrochloride and 325 mg Acetaminophen. It includes warnings about dispensing the correct strength, storage instructions at 20° to 25°C, and child-resistant packaging. The label also shows a 100 tablet count and Rx only designation.*
FDA Label Image

10 mg/325 mg 500 Tablets (10mg 325mg Tabs 500 Nj)

10 mg/325 mg 500 Tablets (10mg 325mg Tabs 500 Nj)
Label for Oxycodone and Acetaminophen Tablets USP, 10 mg*/325 mg strength, supplied in a bulk package of 500 tablets by Halo Pharmaceutical Inc. The label notes the active ingredients with strengths, a caution about multiple strengths, storage instructions, and a barcode with lot and expiration placeholders.*
FDA Label Image

5 mg/325 mg 100 Tablets (5mg 325mg Tabs 100 Nj)

5 mg/325 mg 100 Tablets (5mg 325mg Tabs 100 Nj)
Label for Oxycodone and Acetaminophen Tablets, USP, 5 mg/325 mg, manufactured by Halo Pharmaceutical Inc. The label states tablet strengths, manufacturer address, quantity of 100 tablets, and includes dosage and storage instructions. It features a barcode, NDC number 72022-582-01, and a QR code with lot and expiration date placeholders.*
FDA Label Image

5 mg/325 mg 500 Tablets (5mg 325mg Tabs 500 Nj)

5 mg/325 mg 500 Tablets (5mg 325mg Tabs 500 Nj)
Oxycodone and Acetaminophen Tablets, USP 5 mg*/325 mg bulk package label from Halo Pharmaceutical Inc. It contains 500 tablets, with warnings about multiple strengths and dispensing instructions. Storage conditions recommend keeping the container tightly closed at 20° to 25°C (68° to 77°F). The label includes the NDC 72022-582-05 and notes this is a controlled substance (Schedule II).*
FDA Label Image

7.5 mg/325 mg 100 Tablets (7,5mg 325mg Tabs 100 Nj)

7.5 mg/325 mg 100 Tablets (7,5mg 325mg Tabs 100 Nj)
Label for Oxycodone and Acetaminophen Tablets, USP 7.5 mg/325 mg by Halo Pharmaceutical Inc. The label states the active ingredients with their strengths, prescription-only status, package count of 100 tablets, storage instructions, and a barcode. It includes warnings about dispensing and child-resistant packaging requirements.*
FDA Label Image

7.5 mg/325 mg 500 Tablets (7,5mg 325mg Tabs 500 Nj)

7.5 mg/325 mg 500 Tablets (7,5mg 325mg Tabs 500 Nj)
Oxycodone and Acetaminophen Tablets, USP 7.5 mg*/325 mg label showing a bulk package containing 500 tablets. Label includes active ingredient strengths, storage instructions (20° to 25°C), and a note that it is a Schedule II controlled substance. Manufactured by Halo Pharmaceutical Inc, Whippany, NJ. Barcode and QR code present for tracking.*
FDA Label Image

Acetaminophen Molecule (Acetaminophen Molecule)

Acetaminophen Molecule (Acetaminophen Molecule)
Chemical structure diagram of acetaminophen, showing its molecular formula C8H9NO2 and molecular weight 151.17. This structure includes the acetaminophen core with hydroxyl and amide functional groups.*
FDA Label Image

Oxycodone Molecule (Oxycodone Molecule)

Oxycodone Molecule (Oxycodone Molecule)
Chemical structure of oxycodone hydrochloride, the active ingredient shown with its molecular formula C18H21NO4·HCl and molecular weight 351.82.*

* 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.