Package 69238-2300-1

Brand: oxycodone hcl

Generic: oxycodone hcl
NDC Package

Package Facts

Identity

Package NDC 69238-2300-1
Digits Only 6923823001
Product NDC 69238-2300
Product ID 69238-2300_32e0a011-6ef8-4c45-b080-33acd76a1bea
Description

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69238-2300-1)

Marketing

Marketing Status
Marketed Since 2022-04-01
Brand oxycodone hcl
Generic oxycodone hcl
Sample Package No

Linked Drug Pages (1)

Oxycodone HCl ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "32e0a011-6ef8-4c45-b080-33acd76a1bea", "openfda": {"upc": ["0369238229813", "0369238230017", "0369238229615", "0369238229417"], "unii": ["C1ENJ2TE6C"], "rxcui": ["1860129", "1860137", "1860148", "1860157"], "spl_set_id": ["8220e596-f32e-49cf-a11c-0c79209c3633"], "manufacturer_name": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69238-2300-1)", "package_ndc": "69238-2300-1", "marketing_start_date": "20220401"}], "brand_name": "Oxycodone HCl", "product_id": "69238-2300_32e0a011-6ef8-4c45-b080-33acd76a1bea", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "69238-2300", "dea_schedule": "CII", "generic_name": "Oxycodone HCl", "labeler_name": "Amneal Pharmaceuticals NY LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone HCl", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "80 mg/1"}], "application_number": "NDA022272", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20220401", "listing_expiration_date": "20261231"}