Package 0054-0390-41

Brand: oxycodone hydrochloride

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0054-0390-41
Digits Only 0054039041
Product NDC 0054-0390
Product ID 0054-0390_47e856d4-de7d-49aa-8671-d1b4a35bad4d
Description

15 mL in 1 BOTTLE (0054-0390-41)

Marketing

Marketing Status
Discontinued 2026-08-31
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": "47e856d4-de7d-49aa-8671-d1b4a35bad4d", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049604"], "spl_set_id": ["d8e87c66-f872-4e1d-9ade-ef11490af63b"], "manufacturer_name": ["Hikma Pharmceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "15 mL in 1 BOTTLE (0054-0390-41)", "package_ndc": "0054-0390-41", "marketing_end_date": "20260831", "marketing_start_date": "20140904"}, {"sample": false, "description": "500 mL in 1 BOTTLE (0054-0390-63)", "package_ndc": "0054-0390-63", "marketing_start_date": "20140904"}], "brand_name": "oxycodone hydrochloride", "product_id": "0054-0390_47e856d4-de7d-49aa-8671-d1b4a35bad4d", "dosage_form": "SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0054-0390", "dea_schedule": "CII", "generic_name": "oxycodone hydrochloride", "labeler_name": "Hikma Pharmceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "oxycodone hydrochloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "5 mg/5mL"}], "application_number": "ANDA204037", "marketing_category": "ANDA", "marketing_start_date": "20140904", "listing_expiration_date": "20271231"}