Oxycodone Hydrochloride Tablet
Product Images NDC 0406-8520

18 FDA label images from Specgx Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 18 technical images submitted to the FDA as part of the official labeling for Oxycodone Hydrochloride (NDC 0406-8520). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Specgx 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

Boxed M (Oxycodone Hydrochloride Tablets 1)

Boxed M (Oxycodone Hydrochloride Tablets 1)
OXYCODONE HYDROCHLORIDE 10 mg tablet bottle label manufactured by SpecGx LLC. The label includes the proprietary name, generic name, strength, dosage form, route of administration, and a quantity of 100 tablets per bottle. The label features a white bottle with a white cap and black and yellow text and graphics.*
FDA Label Image

Principal Display Panel 5 mg (Oxycodone Hydrochloride Tablets 10)

Principal Display Panel 5 mg (Oxycodone Hydrochloride Tablets 10)
OXYCODONE HYDROCHLORIDE 10 mg oral tablet packaging label from SpecGx LLC, featuring a single dosage strength of 10 mg. The image shows a white blister pack with tablets arranged in a 3x5 grid format, each tablet and blister cavity visible against the blister backing.*
FDA Label Image

Principal Display Panel 15 mg (Oxycodone Hydrochloride Tablets 11)

Principal Display Panel 15 mg (Oxycodone Hydrochloride Tablets 11)
OXYCODONE HYDROCHLORIDE 30 mg oral tablet with a white round shape and an imprint of letter 'M' on one side, as manufactured by SpecGx LLC. The image shows a single tablet prominently against a white background.*
FDA Label Image

Principal Display Panel 30 mg (Oxycodone Hydrochloride Tablets 12)

Principal Display Panel 30 mg (Oxycodone Hydrochloride Tablets 12)
OXYCODONE HYDROCHLORIDE 30 mg oral tablet packaging label from SpecGx LLC. The image shows a blister pack containing round white tablets with each dose labeled as 30 mg strength. The name oxycodone hydrochloride is prominently displayed along with the dosage form and strength on the packaging.*
FDA Label Image

Oxycodone Hydrochloride Tablets 13

Oxycodone Hydrochloride Tablets 13
Packaging label for OXYCODONE HYDROCHLORIDE 30 mg tablet by SpecGx LLC. The image shows a white round tablet with the imprint 'M' visible on one side, consistent with the 30 mg strength in the oral tablet form.*
FDA Label Image

Oxycodone Hydrochloride Tablets 14

Oxycodone Hydrochloride Tablets 14
Oxycodone Hydrochloride 5 mg oral tablets label for prescription use by SpecGx LLC. The label shows a bottle containing 100 tablets. It includes dosage strength, barcode, NDC 0406-0552-01, directions to see package insert for dosing, medication storage instructions, warnings about moisture and child-resistant packaging, and refill information. The Mallinckrodt trademark is also visible.*
FDA Label Image

Oxycodone Hydrochloride Tablets 15

Oxycodone Hydrochloride Tablets 15
Label for Oxycodone Hydrochloride Tablets USP 10 mg by SpecGx LLC. The label includes a pink tablet image, states 'Rx only,' and indicates the package contains 100 tablets. It provides storage instructions, protection from moisture and light, and notes about pharmacist dispensing requirements. The label also shows NDC 0406-8510-01 and manufacturer location in Webster Groves, MO.*
FDA Label Image

Oxycodone Hydrochloride Tablets 16

Oxycodone Hydrochloride Tablets 16
Oxycodone Hydrochloride 15 mg oral tablets label from SpecGx LLC, containing 100 tablets. The label includes directions for usual dosage, storage instructions, and a warning to protect from moisture and light. It also features a barcode, NDC 0406-8515-01, and identification markings for the tablet sides.*
FDA Label Image

Oxycodone Hydrochloride Tablets 17

Oxycodone Hydrochloride Tablets 17
Label for Oxycodone Hydrochloride 20 mg oral tablets by SpecGx LLC. It shows a bottle containing 100 tablets with NDC 0406-8520-01. The label includes dosage strength, dispensing instructions, storage conditions, and a tamper-evident warning. The product is identified as a Schedule II controlled substance.*
FDA Label Image

Oxycodone Hydrochloride Tablets 18

Oxycodone Hydrochloride Tablets 18
Oxycodone Hydrochloride 30 mg tablets label by SpecGx LLC. The label includes the product name, strength, dosage form (tablet), and prescription status (Rx only). It contains directions to see the package insert for dosage and storage instructions. The label features a barcode, NDC 0406-8530-01, and statements about protecting the product from moisture and light. It also includes warnings about proper container use and dispensing a Medication Guide to patients.*
FDA Label Image

Boxed M (Oxycodone Hydrochloride Tablets 2)

Boxed M (Oxycodone Hydrochloride Tablets 2)
OXYCODONE HYDROCHLORIDE 30 mg oral tablet manufactured by SpecGx LLC. The blister pack shows a single tablet per cavity, arranged in a rectangular grid. The packaging includes labeling with dosage strength and medication name prominently displayed.*
FDA Label Image

Boxed M (Oxycodone Hydrochloride Tablets 3)

Boxed M (Oxycodone Hydrochloride Tablets 3)
OXYCODONE HYDROCHLORIDE oral tablet packaging label displaying multiple strengths: 5 mg, 10 mg, 15 mg, 20 mg, and 30 mg. The label features the SpecGx LLC logo and specifies the product as a human prescription drug. The design emphasizes the brand name and dosage strengths clearly on a blue background.*
FDA Label Image

Chemical Formula (Oxycodone Hydrochloride Tablets 4)

Chemical Formula (Oxycodone Hydrochloride Tablets 4)
The image shows a single white tablet of Oxycodone Hydrochloride with the imprint 'M' on one side. This tablet is an oral dosage form labeled for human prescription use. The labeler is SpecGx LLC, and the product is available in strengths including 5 mg, 10 mg, 15 mg, 20 mg, and 30 mg tablets.*
FDA Label Image

Figure 1 (Oxycodone Hydrochloride Tablets 5)

Figure 1 (Oxycodone Hydrochloride Tablets 5)
OXYCODONE HYDROCHLORIDE 20 mg tablet film-coated, shown as a single oval-shaped yellow tablet imprinted with "M" on one side. The tablet is intended for oral administration. Labeler information is not visible in the image.*
FDA Label Image

Boxed M (Oxycodone Hydrochloride Tablets 6)

Boxed M (Oxycodone Hydrochloride Tablets 6)
Chemical structure of oxycodone hydrochloride, showing the molecular arrangement including aromatic rings, hydroxyl, methoxy, and methyl groups, along with the hydrochloride component. The molecular formula is C18H21NO4 ยท HCl with a molecular weight of 351.82.*
FDA Label Image

Boxed M (Oxycodone Hydrochloride Tablets 7)

Boxed M (Oxycodone Hydrochloride Tablets 7)
A line graph displaying concentration (ng/mL) over time (hours) for oxycodone 5 mg in different quantities (x1, x3, x6). The graph shows how oxycodone concentration changes in the body over a 24-hour period following administration of varying tablet counts.*
FDA Label Image

Boxed M (Oxycodone Hydrochloride Tablets 8)

Boxed M (Oxycodone Hydrochloride Tablets 8)
OXYCODONE HYDROCHLORIDE 10 mg tablets packaging label showing the proprietary name, strength, and dosage form as tablets for oral use. The label includes the SpecGx LLC as the labeler and presents the product as a human prescription drug. It features multiple tablet strengths listed including 5 mg, 10 mg, 15 mg, 20 mg, and 30 mg.*
FDA Label Image

Boxed M (Oxycodone Hydrochloride Tablets 9)

Boxed M (Oxycodone Hydrochloride Tablets 9)
OXYCODONE HYDROCHLORIDE 20 mg oral tablets packaging carton with labeler SpecGx LLC. The front of the carton displays the proprietary name, dosage strength, dosage form, route of administration, and tablet count (100 count). The label includes standard drug and safety-related text.*

* 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.