Package 50268-402-15

{"route": ["ORAL"], "spl_id": "41b02c81-db6d-b522-e063-6394a90abb86", "openfda": {"unii": ["NO70W886KK", "362O9ITL9D"], "rxcui": ["856999", "857002"], "spl_set_id": ["5174bd9a-b777-a6e3-f72f-c16082ee67d3"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-402-15)  / 1 TABLET in 1 BLISTER PACK (50268-402-11)", "package_ndc": "50268-402-15", "marketing_start_date": "20140915"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "50268-402_41b02c81-db6d-b522-e063-6394a90abb86", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "50268-402", "dea_schedule": "CII", "generic_name": "Hydrocodone Bitartrate and Acetaminophen", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrocodone Bitartrate and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "HYDROCODONE BITARTRATE", "strength": "10 mg/1"}], "application_number": "ANDA040736", "marketing_category": "ANDA", "marketing_start_date": "20140915", "listing_expiration_date": "20261231"}