Package 70518-4267-0

{"route": ["ORAL"], "spl_id": "400ab61f-5daf-6925-e063-6394a90ae1f6", "openfda": {"nui": ["N0000175430"], "unii": ["838F01T721"], "rxcui": ["672571"], "spl_set_id": ["f13d3678-a861-42ba-be44-0d89f1b66ef3"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-4267-0)", "package_ndc": "70518-4267-0", "marketing_start_date": "20250127"}, {"sample": false, "description": "30 POUCH in 1 BOX (70518-4267-1)  / 1 TABLET, EXTENDED RELEASE in 1 POUCH (70518-4267-2)", "package_ndc": "70518-4267-1", "marketing_start_date": "20250128"}], "brand_name": "Paliperidone", "product_id": "70518-4267_400ab61f-5daf-6925-e063-6394a90ae1f6", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70518-4267", "generic_name": "Paliperidone", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Paliperidone", "active_ingredients": [{"name": "PALIPERIDONE", "strength": "9 mg/1"}], "application_number": "ANDA205618", "marketing_category": "ANDA", "marketing_start_date": "20250127", "listing_expiration_date": "20261231"}