Package 72578-191-01

{"route": ["ORAL"], "spl_id": "627d9ff9-9d42-4c02-b67d-6de17177cb1a", "openfda": {"nui": ["N0000175430"], "unii": ["838F01T721"], "rxcui": ["672567", "672569", "672571", "866103"], "spl_set_id": ["163898a4-6088-46a0-9253-dd9187c557be"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Viona Pharmaceuticals Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72578-191-01)", "package_ndc": "72578-191-01", "marketing_start_date": "20250601"}, {"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72578-191-05)", "package_ndc": "72578-191-05", "marketing_start_date": "20250601"}, {"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72578-191-06)", "package_ndc": "72578-191-06", "marketing_start_date": "20250601"}], "brand_name": "Paliperidone", "product_id": "72578-191_627d9ff9-9d42-4c02-b67d-6de17177cb1a", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "72578-191", "generic_name": "Paliperidone", "labeler_name": "Viona Pharmaceuticals Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Paliperidone", "active_ingredients": [{"name": "PALIPERIDONE", "strength": "3 mg/1"}], "application_number": "ANDA217445", "marketing_category": "ANDA", "marketing_start_date": "20250601", "listing_expiration_date": "20261231"}