Package 64950-354-50

Brand: oxycodone hydrochloride

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 64950-354-50
Digits Only 6495035450
Product NDC 64950-354
Product ID 64950-354_f06a167a-fef6-4f5e-b7e2-aeb340ddb9d7
Description

1 BOTTLE, PLASTIC in 1 CARTON (64950-354-50) / 500 mL in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2013-09-09
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": "f06a167a-fef6-4f5e-b7e2-aeb340ddb9d7", "openfda": {"upc": ["0364950353037", "0364950354058"], "unii": ["C1ENJ2TE6C"], "rxcui": ["1049604", "1049615"], "spl_set_id": ["6869fec9-1837-4221-afd8-5cc6fadd025d"], "manufacturer_name": ["Genus Lifesciences Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (64950-354-10)  / 100 mL in 1 BOTTLE, PLASTIC", "package_ndc": "64950-354-10", "marketing_start_date": "20130909"}, {"sample": false, "description": "40 CUP, UNIT-DOSE in 1 CASE (64950-354-45)  / 5 mL in 1 CUP, UNIT-DOSE (64950-354-05)", "package_ndc": "64950-354-45", "marketing_start_date": "20130909"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (64950-354-50)  / 500 mL in 1 BOTTLE, PLASTIC", "package_ndc": "64950-354-50", "marketing_start_date": "20130909"}, {"sample": false, "description": "50 CUP, UNIT-DOSE in 1 CASE (64950-354-55)  / 5 mL in 1 CUP, UNIT-DOSE (64950-354-05)", "package_ndc": "64950-354-55", "marketing_start_date": "20130909"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "64950-354_f06a167a-fef6-4f5e-b7e2-aeb340ddb9d7", "dosage_form": "SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "64950-354", "dea_schedule": "CII", "generic_name": "Oxycodone Hydrochloride", "labeler_name": "Genus Lifesciences Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydrochloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "5 mg/5mL"}], "application_number": "NDA200535", "marketing_category": "NDA", "marketing_start_date": "20130909", "listing_expiration_date": "20261231"}