Package 0781-3159-72

{"route": ["INTRAMUSCULAR"], "spl_id": "b2fa51f4-e418-4113-bdd8-17f33ba250b7", "openfda": {"nui": ["N0000175430"], "upc": ["0307813159728"], "unii": ["N7U69T4SZR"], "rxcui": ["485968"], "spl_set_id": ["1e9666ef-4271-4834-8496-ccb3125d83db"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (0781-3159-72)  / 2 mL in 1 VIAL", "package_ndc": "0781-3159-72", "marketing_start_date": "20111024"}], "brand_name": "Olanzapine", "product_id": "0781-3159_b2fa51f4-e418-4113-bdd8-17f33ba250b7", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "0781-3159", "generic_name": "Olanzapine", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine", "active_ingredients": [{"name": "OLANZAPINE", "strength": "10 mg/2mL"}], "application_number": "ANDA201588", "marketing_category": "ANDA", "marketing_start_date": "20111024", "listing_expiration_date": "20261231"}