Roxybond Tablet, Coated
Product Images NDC 81140-101

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Roxybond (NDC 81140-101). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Protega 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

Figure 1 (Rox02 0001 01)

Figure 1 (Rox02 0001 01)
This appears to be a chart or graph with measurements of drug liking VAS (visual analog scale) ranging from 0 to 80 over a span of 24 hours in relation to different types of oxycodone administration. The chart includes measurements for crushed intranasal oxycodone immediate-release tablets, crushed intranasal ROXYBOND, intact oral ROXYBOND, and a placebo. However, there is not enough information to provide further details or conclusions.*
FDA Label Image

Structural Formula (Rox02 0001 02)

FDA Label Image

Figure 2 (Rox02 0001 03)

FDA Label Image

Principal Display Panel – 5 mg Bottle Label (Rox02 0001 04)

Principal Display Panel – 5 mg Bottle Label (Rox02 0001 04)
Each tablet with the identification code "IDT/0 5" contains 5 mg of oxycodone hydrochloride. These tablets, marketed under the brand name RoxyBond™, are indicated for the management of pain severe enough to require an opioid analgesic. The package insert provides complete prescribing information. The tablets should be stored at a temperature range of 15°-30°C (59°-86°F), protected from moisture, in a well-closed container with a child-resistant closure. The National Drug Code (NDC) for the package containing 100 tablets is 81140-101-10. The manufacturer of RoxyBond™ tablets is Protega Pharmaceuticals, LLC, based in Princeton, NJ.*
FDA Label Image

Principal Display Panel – 15 mg Bottle Label (Rox02 0001 05)

Principal Display Panel – 15 mg Bottle Label (Rox02 0001 05)
Each tablet contains 15mg of oxycodone hydrochloride, and this medication is intended for prescription-only dispensation. Patients who receive this medication must be given a medication guide together with this drug. Also, these Oxycodone hydrochloride tablets should be stored in a well-closed container at room temperature between 15° and 30°C. It's important to keep the tablets out of the reach of children and safe from moisture. These tablets are manufactured for Protega Pharmaceuticals LLC, located in Princeton, NJ 08540. For complete prescribing information, interested parties should refer to the package insert.*
FDA Label Image

Principal Display Panel – 30 mg Bottle Label (Rox02 0001 06)

Principal Display Panel – 30 mg Bottle Label (Rox02 0001 06)
Each tablet contains 30mg of Oxycodone Hydrochloride, which is equivalent to 30mg of OxyCodone. The tablets come in a pack of 100 with an identification code. The tablets should be stored at a temperature of 25°C (77°F) with permitted excursions of 15°C to 30°C (59°F to 86°F) as per USP controlled room temperature. The tablets should not be used unless identified. A medication guide needs to accompany the tablets to protect from moisture. The tablets must be dispensed with a child-resistant closure in a well-closed container. This medication is manufactured for Protega Pharmaceuticals, LLC based in Princeton, NJ. For detailed prescribing information, please refer to the package insert.*

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