Oxycodone And Acetaminophen
Product Images NDC 70710-1328

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Oxycodone And Acetaminophen (NDC 70710-1328). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zydus Pharmaceuticals (usa) 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

Oxy Structure (9659dab4 0e5b 4267 9f42 294511ba54e5 01)

Chemical structure of oxycodone hydrochloride, showing the molecular formula C18H21NO4·HCl and molecular weight 351.82. The diagram depicts the ring structures and functional groups of oxycodone with a hydrochloride component.*

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Apap Structure (9659dab4 0e5b 4267 9f42 294511ba54e5 02)

Chemical structure of acetaminophen, showing its molecular formula C8H9NO2 and molecular weight 151.17.*

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2.5 mg/325 mg 100 Count Bottle Label (9659dab4 0e5b 4267 9f42 294511ba54e5 03)

Label for Oxycodone and Acetaminophen tablets, USP with a strength of 2.5 mg/325 mg. The label includes a warning about multiple strengths and dispensing instructions. It also displays the Zydus Pharmaceuticals (USA) Inc. logo and indicates a package size of 100 tablets for prescription use only.*

FDA Label Image

5 mg/325 mg 100 Count Bottle Label (9659dab4 0e5b 4267 9f42 294511ba54e5 04)

Label for Oxycodone and Acetaminophen Tablets, USP showing strength 5 mg*/325 mg. The label notes multiple strengths and instructs pharmacy staff to dispense the accompanying medication guide. Pack contains 100 tablets, Rx only. The labeler is Zydus Pharmaceuticals (USA) Inc.*

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5 mg/325 mg 500 Count Bottle Label (9659dab4 0e5b 4267 9f42 294511ba54e5 05)

Oxycodone and Acetaminophen Tablets, USP, strength 5 mg / 325 mg, labeled by Zydus Pharmaceuticals (USA) Inc. The label includes warnings about multiple strengths and instructs pharmacists to dispense the accompanying Medication Guide. Package contains 500 tablets, Rx only.*

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7.5 mg/325 mg 100 Count Bottle Label (9659dab4 0e5b 4267 9f42 294511ba54e5 06)

The label for Oxycodone and Acetaminophen tablets, USP, shows a strength of 7.5 mg/325 mg. It includes a note advising multiple strengths exist and dispensing only when the strength is stated. The label also directs pharmacists to provide the Medication Guide to each patient. The product is from Zydus Pharmaceuticals (USA) Inc. and the container holds 100 tablets, prescription only.*

FDA Label Image

7.5 mg/325 mg 500 Count Bottle Label (9659dab4 0e5b 4267 9f42 294511ba54e5 07)

Label for Oxycodone and Acetaminophen Tablets USP by Zydus Pharmaceuticals (USA) Inc. The strength shown is 7.5 mg* / 325 mg. The label states multiple strengths are available and instructs not to dispense unless strength is stated. It also directs pharmacists to provide a medication guide to patients. The package contains 500 tablets, Rx only.*

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10 mg/325 mg 100 Count Bottle Label (9659dab4 0e5b 4267 9f42 294511ba54e5 08)

Oxycodone and Acetaminophen Tablets, USP label showing strength 10 mg / 325 mg. The label includes a warning that multiple strengths exist and dispensing requires verifying the strength. It directs pharmacists to dispense the accompanying Medication Guide. The package contains 100 tablets for Rx only and is labeled by Zydus Pharmaceuticals (USA) Inc.*

FDA Label Image

10 mg/325 mg 500 Count Bottle Label (9659dab4 0e5b 4267 9f42 294511ba54e5 09)

Oxycodone and Acetaminophen Tablets USP label with strengths of 10 mg/325 mg. The label includes a warning about multiple strengths and advises pharmacists to dispense the medication guide to each patient. The product is labeled by Zydus Pharmaceuticals (USA) Inc. and is available in a 500-tablet Rx only package.*

* 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.