Package 72865-128-05

{"route": ["ORAL"], "spl_id": "6261bbcf-f814-4219-9954-8f4662cfa9d9", "openfda": {"upc": ["0372865129012", "0372865128015", "0372865128053", "0372865129050"], "unii": ["C1ENJ2TE6C"], "rxcui": ["1049611", "1049618"], "spl_set_id": ["e5c8e72d-4ac5-4ca3-9557-6a659d4d8338"], "manufacturer_name": ["XLCare Pharmaceuticals, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72865-128-01)", "package_ndc": "72865-128-01", "marketing_start_date": "20200225"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (72865-128-05)", "package_ndc": "72865-128-05", "marketing_start_date": "20200225"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "72865-128_6261bbcf-f814-4219-9954-8f4662cfa9d9", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72865-128", "dea_schedule": "CII", "generic_name": "Oxycodone Hydrochloride", "labeler_name": "XLCare Pharmaceuticals, Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydrochloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA207418", "marketing_category": "ANDA", "marketing_start_date": "20200225", "listing_expiration_date": "20261231"}