Package 70000-0479-2

{"route": ["ORAL"], "spl_id": "df386042-7796-4e24-9f8e-39ea465065ad", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0096295136845"], "unii": ["495W7451VQ"], "rxcui": ["310621"], "spl_set_id": ["54a59e95-f95a-4bcd-ac9d-8d4ace85277f"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["CARDINAL HEALTH 110, LLC. DBA LEADER 70000"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "14 BLISTER PACK in 1 CARTON (70000-0479-1)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "70000-0479-1", "marketing_end_date": "20261028", "marketing_start_date": "20190131"}, {"sample": false, "description": "28 BLISTER PACK in 1 CARTON (70000-0479-2)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "70000-0479-2", "marketing_end_date": "20270328", "marketing_start_date": "20190131"}], "brand_name": "Mucus Relief Extended Release Maximum Strength", "product_id": "70000-0479_df386042-7796-4e24-9f8e-39ea465065ad", "dosage_form": "TABLET", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "70000-0479", "generic_name": "Guaifenesin", "labeler_name": "CARDINAL HEALTH 110, LLC. DBA LEADER 70000", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief Extended Release", "brand_name_suffix": "Maximum Strength", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "1200 mg/1"}], "application_number": "ANDA207342", "marketing_category": "ANDA", "marketing_end_date": "20270328", "marketing_start_date": "20190131"}