Package 83324-085-01

{"route": ["ORAL"], "spl_id": "1ac8a196-00fa-a986-e063-6294a90a948f", "openfda": {"upc": ["0635515954618"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["3ce5bbf2-d449-464e-abeb-5c26866d1ab5"], "manufacturer_name": ["CHAIN DRUG MARKETING ASSOCIATION, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (83324-085-01)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "83324-085-01", "marketing_start_date": "20240429"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (83324-085-50)  / 50 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "83324-085-50", "marketing_start_date": "20240429"}], "brand_name": "Pain Relief PM Extra Strength", "product_id": "83324-085_1ac8a196-00fa-a986-e063-6294a90a948f", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "83324-085", "generic_name": "Acetaminophen and Diphenhydramine Hydrochloride", "labeler_name": "CHAIN DRUG MARKETING ASSOCIATION, 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": "20240429", "listing_expiration_date": "20261231"}