Package 57344-203-02

{"route": ["ORAL"], "spl_id": "1acb86a4-a4a9-7ccc-e063-6294a90a67ed", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ"], "rxcui": ["636522"], "spl_set_id": ["68d6b88a-85ed-414d-8369-c7cceb8e9780"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["AAA Pharmaceutical, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (57344-203-02)  / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "57344-203-02", "marketing_start_date": "20240201"}], "brand_name": "Mucus Relief", "product_id": "57344-203_1acb86a4-a4a9-7ccc-e063-6294a90a67ed", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "57344-203", "generic_name": "Guaifenesin", "labeler_name": "AAA Pharmaceutical, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "600 mg/1"}], "application_number": "ANDA213420", "marketing_category": "ANDA", "marketing_start_date": "20240201", "listing_expiration_date": "20261231"}