Package 0135-0608-02

{"route": ["ORAL"], "spl_id": "10c16df6-aa2f-03c3-e063-6294a90a93e5", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189", "1094718"], "spl_set_id": ["01e7dddb-755c-4745-b701-edcdb6209064"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0135-0608-01)  / 24 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0135-0608-01", "marketing_start_date": "20161201"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0135-0608-02)  / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0135-0608-02", "marketing_start_date": "20161201"}, {"sample": false, "description": "50 PACKET in 1 CARTON (0135-0608-03)  / 2 TABLET, FILM COATED in 1 PACKET (0135-0608-04)", "package_ndc": "0135-0608-03", "marketing_start_date": "20161201"}], "brand_name": "PANADOL PM", "product_id": "0135-0608_10c16df6-aa2f-03c3-e063-6294a90a93e5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "0135-0608", "generic_name": "acetaminophen and diphenhydramine HCl", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "PANADOL", "brand_name_suffix": "PM", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20161201", "listing_expiration_date": "20261231"}