Package 0904-6678-40

Brand: oxycodone hydrochloride

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0904-6678-40
Digits Only 0904667840
Product NDC 0904-6678
Description

1 BOTTLE, PLASTIC in 1 CARTON (0904-6678-40) / 500 mL in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2016-11-23
Brand oxycodone hydrochloride
Generic oxycodone hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7386412b-6260-4ac0-a1ce-6ce18d0421e0", "openfda": {"upc": ["0309046678403"], "unii": ["C1ENJ2TE6C"], "rxcui": ["1049604"], "spl_set_id": ["e4fbf3fd-8755-4699-9a61-ba7fada0f93f"], "manufacturer_name": ["MAJOR PHARMACEUTICALS"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (0904-6678-40)  / 500 mL in 1 BOTTLE, PLASTIC", "package_ndc": "0904-6678-40", "marketing_start_date": "20161123"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "0904-6678_7386412b-6260-4ac0-a1ce-6ce18d0421e0", "dosage_form": "SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0904-6678", "dea_schedule": "CII", "generic_name": "Oxycodone Hydrochloride", "labeler_name": "MAJOR PHARMACEUTICALS", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydrochloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "5 mg/5mL"}], "application_number": "ANDA207511", "marketing_category": "ANDA", "marketing_start_date": "20161123", "listing_expiration_date": "20271231"}