Package 59726-734-20

{"route": ["ORAL"], "spl_id": "3e3e9c5d-9d53-4465-98b7-aa5775a2c81c", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0359726731232"], "unii": ["495W7451VQ"], "rxcui": ["636522"], "spl_set_id": ["3c01a88f-35c8-4e43-9997-ebee7943820f"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["P & L Development, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "20 BLISTER PACK in 1 CARTON (59726-734-20)  / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "59726-734-20", "marketing_start_date": "20241206"}], "brand_name": "Mucus Relief", "product_id": "59726-734_3e3e9c5d-9d53-4465-98b7-aa5775a2c81c", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "59726-734", "generic_name": "Guaifenesin", "labeler_name": "P & L Development, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "600 mg/1"}], "application_number": "ANDA207342", "marketing_category": "ANDA", "marketing_start_date": "20241206", "listing_expiration_date": "20261231"}