Package 82725-1012-1

{"route": ["ORAL"], "spl_id": "395687f6-95e4-578c-e063-6394a90a1e6a", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0691036647170"], "unii": ["495W7451VQ"], "rxcui": ["359601"], "spl_set_id": ["26a51b0e-039c-663c-e063-6394a90ad384"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Cabinet Health, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 TABLET in 1 BOTTLE (82725-1012-1)", "package_ndc": "82725-1012-1", "marketing_start_date": "20241101"}], "brand_name": "Mucus Relief", "product_id": "82725-1012_395687f6-95e4-578c-e063-6394a90a1e6a", "dosage_form": "TABLET", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "82725-1012", "generic_name": "Guaifenesin 400 mg", "labeler_name": "Cabinet Health, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "400 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20241101", "listing_expiration_date": "20261231"}