NDC 81140-101

RoxyBond

Oxycodone Hydrochloride

RoxyBond is a Oral Tablet, Coated in the Human Prescription Drug category. It is labeled and distributed by Protega Pharmaceuticals Llc. The primary component is Oxycodone Hydrochloride.

• Product ID: 81140-101_0ee8ef3f-7de0-4071-9c05-4206009ec2fc
• NDC: 81140-101
• Product Type: Human Prescription Drug
• Proprietary Name: RoxyBond
• Generic Name: Oxycodone Hydrochloride
• Dosage Form: Tablet, Coated
• Route of Administration: ORAL
• Marketing Start Date: 2022-03-31
• Marketing Category: NDA /
• Application Number: NDA209777
• Labeler Name: Protega Pharmaceuticals LLC
• Substance Name: OXYCODONE HYDROCHLORIDE
• Active Ingredient Strength: 5 mg/1
• Pharm Classes: Full Opioid Agonists [MoA], Opioid Agonist [EPC]
• DEA Schedule: CII
• NDC Exclude Flag: N
• Listing Certified Through: 2023-12-31

Packaging

NDC 81140-101-10

100 TABLET, COATED in 1 BOTTLE (81140-101-10)

• Marketing Start Date: 2022-03-31
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

NDC Crossover Matching brand name "RoxyBond" or generic name "Oxycodone Hydrochloride"

NDC	Brand Name	Generic Name
65597-502	Roxybond	Roxybond
65597-501	Roxybond	Roxybond
65597-503	Roxybond	Roxybond
0054-0390	oxycodone hydrochloride	oxycodone hydrochloride
0054-0393	Oxycodone Hydrochloride	Oxycodone Hydrochloride
0054-0522	Oxycodone Hydrochloride	Oxycodone Hydrochloride
0093-5731	Oxycodone Hydrochloride	Oxycodone Hydrochloride
0093-5732	Oxycodone Hydrochloride	Oxycodone Hydrochloride
0093-5733	Oxycodone Hydrochloride	Oxycodone Hydrochloride
0093-5734	Oxycodone Hydrochloride	Oxycodone Hydrochloride
0115-1556	OXYCODONE HYDROCHLORIDE	OXYCODONE HYDROCHLORIDE
0115-1557	OXYCODONE HYDROCHLORIDE	OXYCODONE HYDROCHLORIDE
0115-1558	OXYCODONE HYDROCHLORIDE	OXYCODONE HYDROCHLORIDE
0115-1559	OXYCODONE HYDROCHLORIDE	OXYCODONE HYDROCHLORIDE