Package 0054-0390-63
Brand: oxycodone hydrochloride
Generic: oxycodone hydrochloridePackage Facts
Identity
Package NDC
0054-0390-63
Digits Only
0054039063
Product NDC
0054-0390
Description
500 mL in 1 BOTTLE (0054-0390-63)
Marketing
Marketing Status
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": "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"}