Oxycontin Tablet, Film Coated, Extended Release
Product Images NDC 59011-430

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Oxycontin (NDC 59011-430). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Knoa Pharma Llc, 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

FDA Label Image

15 mg

mg and OxyContin, this is a prescription drug label provided by Purdue Pharma LP. The drug is oxycodone hydrochloride, extended-release tablets that must be swallowed whole. The label indicates important safety information such as not cutting, crushing, breaking, or dissolving the tablets. The NDC for this drug is 5001141510.*

FDA Label Image

20 mg

This appears to be a medication label for OxyContin Il which is a brand name for oxycodone hydrochloride. The label includes dosage information and instructions, such as swallowing the tablets whole and not cutting, breaking, chewing, crushing, or disobeying the prescription. It also states that a valid prescription is required for dispensing and includes the NDC (National Drug Code) number and instructions for attention to be paid to the accompanying guide.*

FDA Label Image

30 mg

This text appears to be a prescription drug label for a medication called OxyContin, which comes in 25mg and 30mg extended-release tablets containing oxycodone hydrochloride. The label provides information about the manufacturer (Purdue Pharma LP) and the quantity of tablets (100).*

FDA Label Image

40 mg

This is a prescription drug called OxyContin, which contains oxycodone hydrochloride and is used as an extended-release tablet. The package includes a notice to provide an ethical guide upon dispensing the product. The tablets should not be cut, broken, chewed, crushed, or dissolved and must be taken whole. No further information is available.*

FDA Label Image

60 mg

This text appears to be a medication guide for OxyContin® (oxycodone hydrochloride) extended-release tablets. The guide provides instructions to swallow the tablets whole and not to break, chew, crush or dissolve them. The guide also mentions that a medication guide must be provided to the patient upon dispersing the medication. The text also indicates that this is a prescription medication and that a doctor must prescribe it for the patient.*

FDA Label Image

80 mg

This appears to be a medication guide for OxyContin, which is a brand name for oxycodone hydrochloride extended-release tablets. It includes information such as the dosage instructions and warnings against cutting, breaking, chewing, crushing, or dissolving the tablets. A patient should be provided with this guide when dispensing the medication. The document also has a product code number (NDG 590171-480-10) and indicates that it contains 100 tablets.*

FDA Label Image

Oxycontin Logo

OXYCONTINC is a drug that contains Oxycodone Hydrochloride in extended-release tablet form. This drug is commonly used as a pain reliever but can also be abused due to its potential for addiction.*

FDA Label Image

Figure-1 (Figure 1)

FDA Label Image

Oxycodone-hydrochloride (Oxycodone Hydrochloride)

This is the chemical formula for a compound, likely a type of organic molecule, with the molecular formula CisH21 NOs o HC1 and a molecular weight of 351.83. Without further context, its specific properties or uses cannot be determined.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.