Package 0031-8744-10

{"route": ["ORAL"], "spl_id": "156fd078-37b4-ddce-e063-6294a90ae226", "openfda": {"unii": ["362O9ITL9D", "9D2RTI9KYH", "V9BI9B5YI2"], "rxcui": ["1094549"], "spl_set_id": ["e7cf7c5d-5c9a-4201-9e30-1cd616071855"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 BLISTER PACK in 1 CARTON (0031-8744-10)  / 2 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "0031-8744-10", "marketing_start_date": "20180701"}], "brand_name": "Robitussin Maximum Strength Severe Multi-Symptom 7 in 1 Relief Nighttime", "product_id": "0031-8744_156fd078-37b4-ddce-e063-6294a90ae226", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]", "Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]"], "product_ndc": "0031-8744", "generic_name": "acetaminophen, dextromethorphan hydrobromide, and doxylamine succinate", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Robitussin Maximum Strength Severe Multi-Symptom 7 in 1 Relief Nighttime", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "15 mg/1"}, {"name": "DOXYLAMINE SUCCINATE", "strength": "6.25 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20150701", "listing_expiration_date": "20261231"}