Oxycodone And Acetaminophen Tablet
Product Images NDC 43386-493

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Oxycodone And Acetaminophen (NDC 43386-493). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lupin Pharmaceuticals,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

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FDA Label Image

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FDA Label Image

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This is a pharmaceutical product containing Oxycodone Hydrochloride and Acetaminophen, used as a pain reliever. The tablets come in different strengths, and each one contains 2.5 mg of oxycodone HCl. The product requires a DEA order form and must be stored at 20°C to 25°C. It comes in a light-resistant container with a child-resistant closure. Each patient must receive the accompanying medication guide. This information pertains to Lupin's 100 tablets.*

FDA Label Image

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This is a description of a medication called NDC 43386-490-10. Each tablet contains 2.5 mg of Oxycodone Hydrochloride and 325 mg of Acetaminophen, and it should be stored at Room Temperature (20° to 25°C). It is manufactured by Novel Laboratories and dispensed in a tight, child-resistant container. The medication guide should be given to each patient, and dosage instructions can be found in the package insert. It is available in multiple strengths and should only be dispensed with a stated strength.*

FDA Label Image

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FDA Label Image

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This is a drug with the NDC code 43386-491-10, containing 5mg of Oxycodone Hydrochloride and 325mg of Acetaminophen. It is manufactured by Novel Laboratories, Inc. and is stored at 20° to 25°C (68° to 77°F). The usual dosage is provided in the package insert. It should be dispensed in tight, light-resistant containers with a child-resistant closure. A medication guide should be provided to each patient. Multiple strengths are available, but it should not be dispensed unless the strength is stated.*

FDA Label Image

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This is the prescribing information of Oxycodone and Acetaminophen tablets provided by Lupin Pharmaceuticals. This medication guide should be provided to each patient along with the medicine. The tablets are available in multiple strengths and should not be dispensed unless the strength is stated. Each tablet contains Oxycodone Hydrochloride and Acetaminophen. The tablets come in a container as defined by USP with a child-resistant closure. The tablets must be stored between 20° and 25°C. This medication is manufactured by Novel Laboratories and is intended for use only through a DEA order form.*

FDA Label Image

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This is a description of a prescription drug that contains Oxycodone Hydrochloride and Acetaminophen. The tablets are manufactured by Novel Laboratories Inc, and distributed by Lupin Pharmaceuticals Inc. The usual dosage and complete prescribing information can be found in the package insert. The tablets come in multiple strengths and should be dispensed in a light-resistant container with a child-resistant closure. Please refer to the Medication Guide for each patient. The NDC number for this product is 43386-492-10. The tablets should be stored at 20° to 25°C (68° to 77°F).*

FDA Label Image

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Each tablet of LUPIN 100 contains Oxycodone Hydrochloride, USP 10mg and Acetaminophen = %Tmooloyodons Tablets, USP 25mg. It is advised to store the medication at 20° to 25°C (68° to 77°F). The usual dosage should be consulted on the package insert provided by the manufacturer Lupin Pharmaceuticals, Inc. A complete prescribing information is available at Somerset, NJ 08873. It is a prescription drug dispensed in a child-resistant container and requires a DEA order form. Please refer to the accompanying Medication Guide for use.*

FDA Label Image

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* 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.