Product Images Oxycodone Hydrochloride

View Photos of Packaging, Labels & Appearance

Product Label Images

The following 9 images provide visual information about the product associated with Oxycodone Hydrochloride NDC 0115-1556 by Amneal Pharmaceuticals Of New York Llc, such as packaging, labeling, and the appearance of the drug itself. This resource could be helpful for medical professionals, pharmacists, and patients seeking to verify medication information and ensure they have the correct product.

figure 1 - oxycodone hydrochloride extended release tablets 1

figure 1 - oxycodone hydrochloride extended release tablets 1

This is a graph displaying the percentage reduction in drug liking for Oxycodone HCI Extended-Release Tablets compared to powdered Oxycodone HCI after intranasal administration. The x-axis displays the varying doses, and the y-axis displays the percentage reduction in drug liking. There is no further information available in the given text.*

chemical structure - oxycodone hydrochloride extended release tablets 2

chemical structure - oxycodone hydrochloride extended release tablets 2

10 mg Bottle Label - oxycodone hydrochloride extended release tablets 3

10 mg Bottle Label - oxycodone hydrochloride extended release tablets 3

This is a medication guide for Oxycodone Hydrochloride Extended-Release Tablets. The Attention Dispenser indicates that it must be accompanied by the guide. The NDC number is 0115-1556-01 and it is manufactured by Purdue Pharmaceuticals L.P. The tablets are only available through prescription and the package contains 100 tablets. The document also includes the contact information of the distributor, Amneal Pharmaceuticals LLC.*

15 mg Bottle Label - oxycodone hydrochloride extended release tablets 4

15 mg Bottle Label - oxycodone hydrochloride extended release tablets 4

This is a prescription drug label for Oxycodone Hydrochloride Extended-Release Tablets. The label includes important details such as the NDC code (NDC0115-1557-01), the quantity (100 tablets), and the manufacturer (Purdue Pharmaceuticals L.P.). The label states that it is necessary to provide an accompanying medication guide to the patient. This guide is not available in the text.*

20 mg Bottle Label - oxycodone hydrochloride extended release tablets 5

20 mg Bottle Label - oxycodone hydrochloride extended release tablets 5

This text appears to be a mix of information related to a medication named Oxycodone Hydrochloride, such as its dosage (225) and form (extended-release tablets), its NDC (National Drug Code) product code (0115-1558-01), as well as the name and location of its manufacturer (Purdue Pharmaceuticals, L.P in Wilson, NC) and distributor (Amneal Pharmaceuticals LLC). There is also a reference to a "Dispense & dication Guid" but the content or purpose of this guide is not clear.*

30 mg Bottle Label - oxycodone hydrochloride extended release tablets 6

30 mg Bottle Label - oxycodone hydrochloride extended release tablets 6

This is a medication label for Oxycodone Hydrochloride Extended-Release Tablets. The label includes the NDC number, dosage amounts, manufacturer information, and medication guide requirements.*

40 mg Bottle Label - oxycodone hydrochloride extended release tablets 7

40 mg Bottle Label - oxycodone hydrochloride extended release tablets 7

This is a medication guide for Oxycodone Hydrochloride Extended-Release Tablets that must be provided to the patient upon dispensing. It includes information about the medication and its dosage. The tablets are manufactured by Pure Pharmaceuticals and distributed by Amneal Pharmaceuticals LLC in Bridgewater, NJ.*

60 mg Bottle Label - oxycodone hydrochloride extended release tablets 8

60 mg Bottle Label - oxycodone hydrochloride extended release tablets 8

80 mg Bottle Label - oxycodone hydrochloride extended release tablets 9

80 mg Bottle Label - oxycodone hydrochloride extended release tablets 9

This text is a warning label for Oxycodone Hydrochloride Extended-Release Tablets. It cautions the reader to keep the drug out of reach of children and instructs the dispenser to provide the accompanying medication guide to the patient. It also provides the National Drug Code (NDC) for the medication and the name of the manufacturer and distributor. The text advises the patient to swallow the tablets whole and not to cut, break, chew or dissolve them.*

* The product label images have been analyzed using a combination of traditional computing and machine learning techniques. It should be noted that the descriptions provided may not be entirely accurate as they are experimental in nature. Use the information in this page at your own discretion and risk.