Package 76420-322-30

{"route": ["ORAL"], "spl_id": "32cd8c6c-83cf-fa16-e063-6394a90a6f38", "openfda": {"unii": ["C1ENJ2TE6C", "362O9ITL9D"], "rxcui": ["1049214", "1049221", "1049225", "1049635"], "spl_set_id": ["71c7a627-6ed9-4f49-8cdc-b3228c021e64"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (76420-322-01)", "package_ndc": "76420-322-01", "marketing_start_date": "20250415"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (76420-322-05)", "package_ndc": "76420-322-05", "marketing_start_date": "20250415"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (76420-322-30)", "package_ndc": "76420-322-30", "marketing_start_date": "20250415"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (76420-322-60)", "package_ndc": "76420-322-60", "marketing_start_date": "20250415"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (76420-322-90)", "package_ndc": "76420-322-90", "marketing_start_date": "20250415"}], "brand_name": "OXYCODONE AND ACETAMINOPHEN", "product_id": "76420-322_32cd8c6c-83cf-fa16-e063-6394a90a6f38", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "76420-322", "dea_schedule": "CII", "generic_name": "Oxycodone and Acetaminophen", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXYCODONE AND ACETAMINOPHEN", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "OXYCODONE HYDROCHLORIDE", "strength": "7.5 mg/1"}], "application_number": "ANDA207419", "marketing_category": "ANDA", "marketing_start_date": "20170411", "listing_expiration_date": "20261231"}