Package 76420-897-90

{"route": ["ORAL"], "spl_id": "2b35649b-3399-ef25-e063-6294a90a1efb", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049611", "1049618", "1049621", "1049683", "1049686"], "spl_set_id": ["c10cc127-8756-4ddc-9f46-1e003ef271dc"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (76420-897-01)", "package_ndc": "76420-897-01", "marketing_start_date": "20250108"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE, PLASTIC (76420-897-10)", "package_ndc": "76420-897-10", "marketing_start_date": "20250108"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (76420-897-20)", "package_ndc": "76420-897-20", "marketing_start_date": "20250108"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (76420-897-30)", "package_ndc": "76420-897-30", "marketing_start_date": "20250108"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (76420-897-60)", "package_ndc": "76420-897-60", "marketing_start_date": "20250108"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (76420-897-90)", "package_ndc": "76420-897-90", "marketing_start_date": "20250108"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "76420-897_2b35649b-3399-ef25-e063-6294a90a1efb", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "76420-897", "dea_schedule": "CII", "generic_name": "Oxycodone Hydrochloride", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydrochloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA091490", "marketing_category": "ANDA", "marketing_start_date": "20140908", "listing_expiration_date": "20261231"}