Package 0378-0211-05

{"route": ["ORAL"], "spl_id": "efc5a530-785e-4b88-80e9-00c92e2f1fd4", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["6RZ6XEZ3CR", "26LUD4JO9K"], "rxcui": ["856769", "856792"], "spl_set_id": ["66a756f2-ac77-451c-a19a-08896d73b15c"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0211-01)", "package_ndc": "0378-0211-01", "marketing_start_date": "19861210"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0211-05)", "package_ndc": "0378-0211-05", "marketing_start_date": "19861210"}], "brand_name": "Chlordiazepoxide and Amitriptyline Hydrochloride", "product_id": "0378-0211_efc5a530-785e-4b88-80e9-00c92e2f1fd4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]", "Tricyclic Antidepressant [EPC]"], "product_ndc": "0378-0211", "dea_schedule": "CIV", "generic_name": "chlordiazepoxide and amitriptyline hydrochloride", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlordiazepoxide and Amitriptyline Hydrochloride", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "14 mg/1"}, {"name": "CHLORDIAZEPOXIDE", "strength": "5 mg/1"}], "application_number": "ANDA071297", "marketing_category": "ANDA", "marketing_start_date": "19861210", "listing_expiration_date": "20261231"}