Package 68998-195-02

{"route": ["ORAL"], "spl_id": "252639e3-38cf-04f0-e063-6294a90a94ad", "openfda": {"upc": ["0099581910303"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["e221bbce-83de-0f03-e053-2995a90abca5"], "manufacturer_name": ["MARC GLASSMAN, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (68998-195-02)  / 50 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "68998-195-02", "marketing_start_date": "20221005"}], "brand_name": "Pain Relief PM Extra Strength", "product_id": "68998-195_252639e3-38cf-04f0-e063-6294a90a94ad", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "68998-195", "generic_name": "Acetaminophen and Diphenhydramine Hydrochloride", "labeler_name": "MARC GLASSMAN, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Relief PM", "brand_name_suffix": "Extra Strength", "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": "20221005", "listing_expiration_date": "20261231"}