Package 81522-203-02

{"route": ["ORAL"], "spl_id": "f212f808-9349-2b65-e053-2995a90a5775", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ"], "rxcui": ["636522"], "spl_set_id": ["ec6b5d2f-6568-08d8-e053-2995a90a4d4b"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["FSA STORE INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (81522-203-02)  / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "81522-203-02", "marketing_start_date": "20230111"}], "brand_name": "Mucus Relief", "product_id": "81522-203_f212f808-9349-2b65-e053-2995a90a5775", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "81522-203", "generic_name": "Guaifenesin", "labeler_name": "FSA STORE 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": "20230111", "listing_expiration_date": "20261231"}