Package 59651-418-55

{"route": ["ORAL"], "spl_id": "0004a0bb-87c0-46f8-b36a-95c98107395d", "openfda": {"unii": ["82269ASB48"], "rxcui": ["636671", "636676", "749289"], "spl_set_id": ["0004a0bb-87c0-46f8-b36a-95c98107395d"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (59651-418-55)  / 56 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "59651-418-55", "marketing_start_date": "20250502"}, {"sample": false, "description": "56 TABLET, FILM COATED in 1 BOTTLE (59651-418-56)", "package_ndc": "59651-418-56", "marketing_start_date": "20250502"}], "brand_name": "Varenicline", "product_id": "59651-418_0004a0bb-87c0-46f8-b36a-95c98107395d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinergic Agonists [MoA]", "Cholinergic Receptor Agonist [EPC]", "Partial Cholinergic Nicotinic Agonist [EPC]", "Partial Cholinergic Nicotinic Agonists [MoA]"], "product_ndc": "59651-418", "generic_name": "Varenicline", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Varenicline", "active_ingredients": [{"name": "VARENICLINE TARTRATE", "strength": "1 mg/1"}], "application_number": "ANDA214595", "marketing_category": "ANDA", "marketing_start_date": "20250502", "listing_expiration_date": "20261231"}