Package 81140-101-10

Brand: roxybond

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 81140-101-10
Digits Only 8114010110
Product NDC 81140-101
Description

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

Marketing

Marketing Status
Marketed Since 2023-12-19
Brand roxybond
Generic oxycodone hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "484b1240-1832-049e-e063-6394a90aaa6a", "openfda": {"upc": ["0381140104101", "0381140102107", "0381140101100", "0381140103104"], "unii": ["C1ENJ2TE6C"], "rxcui": ["1944529", "1944535", "1944538", "1944540", "1944541", "1944543", "2693194", "2693196"], "spl_set_id": ["72398542-8e0a-47b2-afeb-9ca5a1f15083"], "manufacturer_name": ["Protega Pharmaceuticals Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (81140-101-10)", "package_ndc": "81140-101-10", "marketing_start_date": "20231219"}], "brand_name": "RoxyBond", "product_id": "81140-101_484b1240-1832-049e-e063-6394a90aaa6a", "dosage_form": "TABLET, COATED", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "81140-101", "dea_schedule": "CII", "generic_name": "Oxycodone hydrochloride", "labeler_name": "Protega Pharmaceuticals Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "RoxyBond", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "NDA209777", "marketing_category": "NDA", "marketing_start_date": "20170420", "listing_expiration_date": "20271231"}