Package 11822-0732-6

{"route": ["ORAL"], "spl_id": "b279a2d1-7941-4862-8f85-d098ded81b05", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0011822739030"], "unii": ["495W7451VQ"], "rxcui": ["310621"], "spl_set_id": ["73184b46-7345-45ed-bac7-b15d5473dba9"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Rite Aid Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "42 BLISTER PACK in 1 CARTON (11822-0732-6)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "11822-0732-6", "marketing_end_date": "20260228", "marketing_start_date": "20190531"}], "brand_name": "Mucus Relief Maximum Strength", "product_id": "11822-0732_b279a2d1-7941-4862-8f85-d098ded81b05", "dosage_form": "TABLET", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "11822-0732", "generic_name": "Guaifenesin", "labeler_name": "Rite Aid Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief", "brand_name_suffix": "Maximum Strength", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "1200 mg/1"}], "application_number": "ANDA207342", "marketing_category": "ANDA", "marketing_end_date": "20260228", "marketing_start_date": "20190531"}