Package 41520-732-14

{"route": ["ORAL"], "spl_id": "72cc5e09-dd68-4158-935a-4fa739235045", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0341520004810"], "unii": ["495W7451VQ"], "rxcui": ["310621"], "spl_set_id": ["c94e3943-20da-4bd4-b0ff-6aa60b03a1bf"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Care One (American Sales Company)"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "14 BLISTER PACK in 1 CARTON (41520-732-14)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "41520-732-14", "marketing_start_date": "20181231"}], "brand_name": "Mucus Relief Maximum Strength", "product_id": "41520-732_72cc5e09-dd68-4158-935a-4fa739235045", "dosage_form": "TABLET", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "41520-732", "generic_name": "Guaifenesin", "labeler_name": "Care One (American Sales Company)", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief", "brand_name_suffix": "Maximum Strength", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "1200 mg/1"}], "application_number": "ANDA207342", "marketing_category": "ANDA", "marketing_start_date": "20181231", "listing_expiration_date": "20261231"}