Package 0378-0442-01

{"route": ["ORAL"], "spl_id": "a0ce12cc-6720-4bbe-9e86-41feb8e6d4cd", "openfda": {"nui": ["N0000175746", "M0016525"], "unii": ["26LUD4JO9K", "FTA7XXY4EZ"], "rxcui": ["856706", "856720", "856797", "856825", "856840"], "spl_set_id": ["e2937445-c015-c9a5-52f8-a2959da97290"], "pharm_class_cs": ["Phenothiazines [CS]"], "pharm_class_epc": ["Phenothiazine [EPC]"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0442-01)", "package_ndc": "0378-0442-01", "marketing_start_date": "19881110"}], "brand_name": "Perphenazine and Amitriptyline Hydrochloride", "product_id": "0378-0442_a0ce12cc-6720-4bbe-9e86-41feb8e6d4cd", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]", "Tricyclic Antidepressant [EPC]"], "product_ndc": "0378-0442", "generic_name": "perphenazine and amitriptyline hydrochloride", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Perphenazine and Amitriptyline Hydrochloride", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "25 mg/1"}, {"name": "PERPHENAZINE", "strength": "2 mg/1"}], "application_number": "ANDA071443", "marketing_category": "ANDA", "marketing_start_date": "19881110", "listing_expiration_date": "20261231"}