Package 70095-020-02

{"route": ["ORAL"], "spl_id": "6ce4dc4f-ad08-424e-b90d-400de0b7050a", "openfda": {"upc": ["0370095019011", "0370095020017"], "unii": ["UR59KN573L"], "rxcui": ["854901", "854905"], "spl_set_id": ["7556f457-c4d3-49d6-b383-0ade6d489091"], "manufacturer_name": ["Sun Pharmaceutical Industries Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, UNIT-DOSE (70095-020-01)", "package_ndc": "70095-020-01", "marketing_start_date": "20240310"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (70095-020-02)", "package_ndc": "70095-020-02", "marketing_start_date": "20240310"}], "brand_name": "BISOPROLOL FUMARATE", "product_id": "70095-020_6ce4dc4f-ad08-424e-b90d-400de0b7050a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70095-020", "generic_name": "BISOPROLOL FUMARATE", "labeler_name": "Sun Pharmaceutical Industries Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BISOPROLOL FUMARATE", "active_ingredients": [{"name": "BISOPROLOL FUMARATE", "strength": "5 mg/1"}], "application_number": "ANDA217617", "marketing_category": "ANDA", "marketing_start_date": "20240310", "listing_expiration_date": "20261231"}