Oxycontin Tablet, Film Coated, Extended Release
Product Images NDC 59011-440

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Oxycontin (NDC 59011-440). 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

10 mg
OxyContin 10 mg extended-release tablets label showing the brand and generic name oxycodone hydrochloride, strength 10 mg, dosage form film-coated tablets. The label includes dispenser attention instructions, tablet count of 100, prescription-only status, labeler Purdue Pharma L.P., and storage instructions with a barcode.*
FDA Label Image

15 mg

15 mg
OxyContin 15 mg extended-release film-coated tablets label by Purdue Pharma L.P. The label displays the product name, strength (15 mg), and dosage form. It includes instructions to swallow tablets whole and important dispenser information. The package contains 100 tablets and is Rx only.*
FDA Label Image

20 mg

20 mg
Label for OxyContin 20 mg extended-release tablets with the active ingredient oxycodone hydrochloride. The label indicates a package size of 100 tablets, prescription only, distributed by Purdue Pharma L.P., Stamford, CT. There is a warning to the dispenser about providing the Medication Guide and instructions to dispense in a tight, light-resistant container. A barcode and NDC number 59011-420-10 are also visible.*
FDA Label Image

30 mg

30 mg
OxyContin 30 mg extended-release tablets label displaying oxycodone hydrochloride as the active ingredient. The label indicates a package containing 100 film-coated, oral extended-release tablets. It includes the NDC 59011-430-10, instructions to provide a medication guide with dispensing, and manufacturer information for Purdue Pharma L.P. and Knoa Pharma LLC.*
FDA Label Image

40 mg

40 mg
Label for OxyContin 40 mg extended-release tablets containing oxycodone hydrochloride. The film-coated tablets come in a bottle of 100 tablets for oral use, labeled as prescription only. The product is manufactured by Purdue Pharma L.P. with NDC 59011-440-10. Directions include usual dosage and cautions against breaking or crushing tablets.*
FDA Label Image

60 mg

60 mg
OxyContin 60 mg extended-release tablets containing oxycodone hydrochloride in film-coated oral tablet form. The label indicates a quantity of 100 tablets, prescription only. Labeler is Knoa Pharma LLC, with a note to accompanying medication guide provision and a barcode present on the label.*
FDA Label Image

80 mg

80 mg
OxyContin 80 mg extended-release tablets, film coated, containing oxycodone hydrochloride. The label shows a package of 100 tablets for oral use by opioid-tolerant patients only. It includes dispensing and dosage instructions, an NDC number, and manufacturer details from Knoa Pharma LLC.*
FDA Label Image
FDA Label Image

Figure-1 (Figure 1)

Figure-1 (Figure 1)
A line graph depicting the percentage reduction in drug liking for finely crushed OxyContin compared to powdered oxycodone hydrochloride following intranasal administration. The x-axis shows percent reduction categories, and the y-axis represents the percentage of subjects, illustrating the decrease in liking as reduction percentage increases.*
FDA Label Image

Oxycodone-hydrochloride (Oxycodone Hydrochloride)

Oxycodone-hydrochloride (Oxycodone Hydrochloride)
Chemical structure diagram of oxycodone hydrochloride, showing its molecular composition and arrangement with the molecular weight 351.83.*

* 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.