Package 0378-7303-53

{"spl_id": "931f0bbe-68fa-5010-6d73-7f97e3d9eddf", "openfda": {"rxcui": ["259176", "1358762", "1359130", "1359131", "1359132"], "spl_set_id": ["054917fa-573b-4b16-a719-ece6c0909656"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 POUCH in 1 CARTON (0378-7303-53)  / 1 BLISTER PACK in 1 POUCH (0378-7303-85)  / 1 KIT in 1 BLISTER PACK *  7 TABLET in 1 BLISTER PACK (0378-7191-71)  *  9 TABLET in 1 BLISTER PACK (0378-7192-59)  *  7 TABLET in 1 BLISTER PACK (0378-7193-71)  *  5 TABLET in 1 BLISTER PACK (0378-7190-98)", "package_ndc": "0378-7303-53", "marketing_start_date": "20220727"}], "brand_name": "NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL AND FERROUS FUMARATE", "product_id": "0378-7303_931f0bbe-68fa-5010-6d73-7f97e3d9eddf", "dosage_form": "KIT", "product_ndc": "0378-7303", "generic_name": "norethindrone acetate and ethinyl estradiol and ferrous fumarate", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL AND FERROUS FUMARATE", "application_number": "ANDA205069", "marketing_category": "ANDA", "marketing_start_date": "20220727", "listing_expiration_date": "20261231"}