Package 50844-519-20

{"route": ["ORAL"], "spl_id": "9f5e3344-4f7b-4096-a4f0-929e140c175c", "openfda": {"upc": ["0050844519213"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["72babe91-2586-4f05-ae90-6debfd23aa5d"], "manufacturer_name": ["L.N.K. International, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE, PLASTIC (50844-519-12)", "package_ndc": "50844-519-12", "marketing_start_date": "20231114"}, {"sample": false, "description": "225 TABLET, COATED in 1 BOTTLE, PLASTIC (50844-519-20)", "package_ndc": "50844-519-20", "marketing_start_date": "20231114"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (50844-519-21)  / 16 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "50844-519-21", "marketing_start_date": "20040510"}], "brand_name": "Pain Reliever Extra Strength", "product_id": "50844-519_9f5e3344-4f7b-4096-a4f0-929e140c175c", "dosage_form": "TABLET, COATED", "product_ndc": "50844-519", "generic_name": "Acetaminophen", "labeler_name": "L.N.K. International, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Reliever", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20040510", "listing_expiration_date": "20261231"}