Package 0135-0620-01

{"route": ["ORAL"], "spl_id": "10c0dc3d-12b7-e9da-e063-6394a90a5dcf", "openfda": {"nui": ["N0000175739", "N0000175729", "N0000175790", "M0023046"], "unii": ["362O9ITL9D", "3G6A5W338E"], "rxcui": ["307686", "1872075"], "spl_set_id": ["e5c2d88a-d903-4ca0-b895-f27e791dfc4e"], "pharm_class_cs": ["Xanthines [CS]"], "pharm_class_pe": ["Central Nervous System Stimulation [PE]"], "pharm_class_epc": ["Central Nervous System Stimulant [EPC]", "Methylxanthine [EPC]"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0135-0620-01)  / 24 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0135-0620-01", "marketing_start_date": "20170301"}], "brand_name": "PANADOL Extra", "product_id": "0135-0620_10c0dc3d-12b7-e9da-e063-6394a90a5dcf", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]", "Methylxanthine [EPC]", "Xanthines [CS]"], "product_ndc": "0135-0620", "generic_name": "acetaminophen and caffeine", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "PANADOL", "brand_name_suffix": "Extra", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}, {"name": "CAFFEINE", "strength": "65 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20170301", "listing_expiration_date": "20261231"}