Package 16103-379-04

{"route": ["ORAL"], "spl_id": "3038393b-2c7b-4f5d-8b5d-d6054f663336", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ"], "rxcui": ["359601"], "spl_set_id": ["0bf70fb4-d3c8-476d-b864-4eadc697a7d8"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Pharbest Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (16103-379-04)  / 30 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "16103-379-04", "marketing_start_date": "20180501"}], "brand_name": "GUAIFENESIN", "product_id": "16103-379_3038393b-2c7b-4f5d-8b5d-d6054f663336", "dosage_form": "TABLET", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "16103-379", "generic_name": "GUAIFENESIN", "labeler_name": "Pharbest Pharmaceuticals, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "GUAIFENESIN", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "400 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180501", "listing_expiration_date": "20261231"}