Package 65162-115-03

{"route": ["ORAL"], "spl_id": "1b44ad7b-ee24-499c-9814-24a95779a97f", "openfda": {"unii": ["362O9ITL9D", "NO70W886KK"], "rxcui": ["857005"], "spl_set_id": ["e23d135c-7aea-405a-804e-5c4f82179e96"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (65162-115-03)", "package_ndc": "65162-115-03", "marketing_start_date": "20160630"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (65162-115-10)", "package_ndc": "65162-115-10", "marketing_start_date": "20160630"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (65162-115-11)", "package_ndc": "65162-115-11", "marketing_start_date": "20160630"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (65162-115-50)", "package_ndc": "65162-115-50", "marketing_start_date": "20160630"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "65162-115_1b44ad7b-ee24-499c-9814-24a95779a97f", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "65162-115", "dea_schedule": "CII", "generic_name": "Hydrocodone Bitartrate and Acetaminophen", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrocodone Bitartrate and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "HYDROCODONE BITARTRATE", "strength": "7.5 mg/1"}], "application_number": "ANDA040746", "marketing_category": "ANDA", "marketing_start_date": "20160630", "listing_expiration_date": "20261231"}