Package 68180-876-73

{"route": ["ORAL"], "spl_id": "21d08d75-2957-4610-94c1-76c844ba2f1b", "openfda": {"nui": ["M0447349", "N0000175602"], "upc": ["0368180876717"], "unii": ["T18F433X4S"], "rxcui": ["198042", "748961"], "spl_set_id": ["121fbf86-1d76-4579-be2f-be9a957b23ab"], "pharm_class_cs": ["Progesterone Congeners [CS]"], "pharm_class_epc": ["Progestin [EPC]"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (68180-876-73)  / 28 TABLET in 1 BLISTER PACK", "package_ndc": "68180-876-73", "marketing_start_date": "20201111"}], "brand_name": "NORETHINDRONE", "product_id": "68180-876_21d08d75-2957-4610-94c1-76c844ba2f1b", "dosage_form": "TABLET", "pharm_class": ["Progesterone Congeners [CS]", "Progestin [EPC]"], "product_ndc": "68180-876", "generic_name": "NORETHINDRONE", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NORETHINDRONE", "active_ingredients": [{"name": "NORETHINDRONE", "strength": ".35 mg/1"}], "application_number": "ANDA091325", "marketing_category": "ANDA", "marketing_start_date": "20201111", "listing_expiration_date": "20261231"}