Package 30142-068-07

{"route": ["ORAL"], "spl_id": "b65ad8d1-ef17-490d-96c0-0ea6096bf684", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["b96a2280-ec4f-7c61-e053-2995a90a18bb"], "manufacturer_name": ["KROGER COMPANY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (30142-068-07)  / 24 TABLET in 1 BOTTLE", "package_ndc": "30142-068-07", "marketing_start_date": "20210204"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (30142-068-24)  / 100 TABLET in 1 BOTTLE", "package_ndc": "30142-068-24", "marketing_start_date": "20240422"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (30142-068-35)  / 225 TABLET in 1 BOTTLE", "package_ndc": "30142-068-35", "marketing_start_date": "20210426"}], "brand_name": "Acetaminophen Extra Strength", "product_id": "30142-068_b65ad8d1-ef17-490d-96c0-0ea6096bf684", "dosage_form": "TABLET", "product_ndc": "30142-068", "generic_name": "Acetaminophen", "labeler_name": "KROGER COMPANY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210204", "listing_expiration_date": "20261231"}