Package 41520-956-09

{"route": ["ORAL"], "spl_id": "f65e2b45-16d7-4186-a2e6-6d0e8724a723", "openfda": {"upc": ["0341520319624"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["fdd7ce80-d6be-41b9-affd-d024cf306b50"], "manufacturer_name": ["FOODHOLD U.S.A., LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (41520-956-09)  / 20 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "41520-956-09", "marketing_start_date": "20071217"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (41520-956-31)  / 80 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "41520-956-31", "marketing_start_date": "20071217"}], "brand_name": "Acetaminophen PM Extra Strength", "product_id": "41520-956_f65e2b45-16d7-4186-a2e6-6d0e8724a723", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "41520-956", "generic_name": "Acetaminophen, Diphenhydramine HCl", "labeler_name": "FOODHOLD U.S.A., LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen 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": "20071217", "listing_expiration_date": "20261231"}