Package 10135-789-01

{"route": ["ORAL"], "spl_id": "437e388b-2293-0064-e063-6394a90add05", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ"], "rxcui": ["197741"], "spl_set_id": ["13b8f480-d1ac-d70c-e063-6394a90ab4f4"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Marlex Pharmaceuticals Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (10135-789-01)", "package_ndc": "10135-789-01", "marketing_start_date": "20240301"}], "brand_name": "Guaifenesin 200mg", "product_id": "10135-789_437e388b-2293-0064-e063-6394a90add05", "dosage_form": "TABLET", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "10135-789", "generic_name": "Guaifenesin", "labeler_name": "Marlex Pharmaceuticals Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Guaifenesin 200mg", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "200 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240301", "listing_expiration_date": "20261231"}