Package 0406-8530-23

Brand: oxycodone hydrochloride

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0406-8530-23
Digits Only 0406853023
Product NDC 0406-8530
Product ID 0406-8530_48d2db7c-2e64-4425-86a5-3ad5289fb7b7
Description

1 TABLET in 1 BLISTER PACK (0406-8530-23)

Marketing

Marketing Status
Marketed Since 2004-06-30
Brand oxycodone hydrochloride
Generic oxycodone hydrochloride
Sample Package No

Linked Drug Pages (1)

OXYCODONE HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "48d2db7c-2e64-4425-86a5-3ad5289fb7b7", "openfda": {"upc": ["0304068515019", "0304068520013", "0304068510014", "0304068530012", "0304060552012"], "unii": ["C1ENJ2TE6C"], "spl_set_id": ["928227bf-89c5-4c64-9823-0e84cc669388"], "manufacturer_name": ["SpecGx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0406-8530-01)", "package_ndc": "0406-8530-01", "marketing_start_date": "20040630"}, {"sample": false, "description": "1 TABLET in 1 BLISTER PACK (0406-8530-23)", "package_ndc": "0406-8530-23", "marketing_start_date": "20040630"}, {"sample": false, "description": "100 TABLET in 1 BLISTER PACK (0406-8530-62)", "package_ndc": "0406-8530-62", "marketing_start_date": "20040630"}], "brand_name": "OXYCODONE HYDROCHLORIDE", "product_id": "0406-8530_48d2db7c-2e64-4425-86a5-3ad5289fb7b7", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0406-8530", "dea_schedule": "CII", "generic_name": "oxycodone hydrochloride", "labeler_name": "SpecGx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXYCODONE HYDROCHLORIDE", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA076758", "marketing_category": "ANDA", "marketing_start_date": "20040630", "listing_expiration_date": "20261231"}