Package 69953-515-01

{"route": ["ORAL"], "spl_id": "677aa953-3c31-4ce5-e053-2991aa0ab2b2", "openfda": {"nui": ["N0000175830", "M0447349", "N0000175602", "N0000175832"], "upc": ["0369953515017"], "unii": ["5W7SIA7YZW"], "rxcui": ["483325", "1657617"], "spl_set_id": ["677aa953-3c30-4ce5-e053-2991aa0ab2b2"], "pharm_class_cs": ["Progesterone Congeners [CS]"], "pharm_class_pe": ["Inhibit Ovum Fertilization [PE]"], "pharm_class_epc": ["Progestin [EPC]", "Progestin-containing Intrauterine System [EPC]"], "manufacturer_name": ["Rapha Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (69953-515-01)  / 1 mg in 1 BLISTER PACK", "package_ndc": "69953-515-01", "marketing_start_date": "20180322"}], "brand_name": "Morning After", "product_id": "69953-515_677aa953-3c31-4ce5-e053-2991aa0ab2b2", "dosage_form": "TABLET", "pharm_class": ["Inhibit Ovum Fertilization [PE]", "Progesterone Congeners [CS]", "Progesterone Congeners [CS]", "Progestin [EPC]", "Progestin-containing Intrauterine Device [EPC]"], "product_ndc": "69953-515", "generic_name": "Levonorgestrel", "labeler_name": "Rapha Pharmaceuticals, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Morning After", "active_ingredients": [{"name": "LEVONORGESTREL", "strength": "1.5 mg/1.5mg"}], "application_number": "ANDA206867", "marketing_category": "ANDA", "marketing_start_date": "20180322", "listing_expiration_date": "20261231"}