Package 60290-077-02

{"route": ["ORAL"], "spl_id": "48e02d69-578d-6c15-e063-6394a90ade7c", "openfda": {"unii": ["82269ASB48"], "rxcui": ["636671", "636676"], "spl_set_id": ["f2e57493-d099-4055-8e92-67611c8d20f4"], "manufacturer_name": ["Umedica Laboratories USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "56 TABLET in 1 BOTTLE (60290-077-01)", "package_ndc": "60290-077-01", "marketing_start_date": "20260109"}, {"sample": false, "description": "60 BLISTER PACK in 1 CARTON (60290-077-02)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "60290-077-02", "marketing_start_date": "20260109"}], "brand_name": "VARENICLINE", "product_id": "60290-077_48e02d69-578d-6c15-e063-6394a90ade7c", "dosage_form": "TABLET", "pharm_class": ["Cholinergic Agonists [MoA]", "Cholinergic Receptor Agonist [EPC]", "Partial Cholinergic Nicotinic Agonist [EPC]", "Partial Cholinergic Nicotinic Agonists [MoA]"], "product_ndc": "60290-077", "generic_name": "VARENICLINE", "labeler_name": "Umedica Laboratories USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VARENICLINE", "active_ingredients": [{"name": "VARENICLINE TARTRATE", "strength": ".5 mg/1"}], "application_number": "ANDA218985", "marketing_category": "ANDA", "marketing_start_date": "20260109", "listing_expiration_date": "20271231"}