Package 50580-374-01

{"spl_id": "21719087-b7ff-e583-e063-6394a90aa10c", "openfda": {"upc": ["0300450149244"], "rxcui": ["1089968", "1250743", "2558505"], "spl_set_id": ["712ba011-79aa-469b-9f0f-04a0b4b705bd"], "manufacturer_name": ["Kenvue Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 PACKAGE (50580-374-01)  *  2 BLISTER PACK in 1 CARTON / 8 TABLET, FILM COATED in 1 BLISTER PACK *  2 BLISTER PACK in 1 CARTON / 4 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "50580-374-01", "marketing_start_date": "20210621"}], "brand_name": "Extra Strength TYLENOL Cold plus Flu Multi-Action Day/Night", "product_id": "50580-374_21719087-b7ff-e583-e063-6394a90aa10c", "dosage_form": "KIT", "product_ndc": "50580-374", "generic_name": "acetaminophen, pseudoephedrine hydrochloride, dextromethorphan hydrobromide, and chlorpheniramine maleate", "labeler_name": "Kenvue Brands LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Extra Strength TYLENOL Cold plus Flu Multi-Action", "brand_name_suffix": "Day/Night", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210621", "listing_expiration_date": "20261231"}