Package 35356-801-30

{"route": ["ORAL"], "spl_id": "378ca952-250f-4c56-a263-d6925c341dd6", "openfda": {"unii": ["362O9ITL9D", "C1ENJ2TE6C"], "rxcui": ["1049214", "1049225"], "spl_set_id": ["bbbc5dc1-5a91-4430-adcb-a5f6963cc0a2"], "manufacturer_name": ["Quality Care Products, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (35356-801-30)", "package_ndc": "35356-801-30", "marketing_end_date": "20260430", "marketing_start_date": "20130910"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (35356-801-60)", "package_ndc": "35356-801-60", "marketing_end_date": "20260430", "marketing_start_date": "20130910"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (35356-801-90)", "package_ndc": "35356-801-90", "marketing_end_date": "20260430", "marketing_start_date": "20130910"}], "brand_name": "Oxycodone and Acetaminophen", "product_id": "35356-801_378ca952-250f-4c56-a263-d6925c341dd6", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "35356-801", "dea_schedule": "CII", "generic_name": "Oxycodone and Acetaminophen", "labeler_name": "Quality Care Products, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "OXYCODONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA202677", "marketing_category": "ANDA", "marketing_end_date": "20260430", "marketing_start_date": "20120802"}