Package 37808-733-40

{"route": ["ORAL"], "spl_id": "d2aca5b5-2bb6-41b5-a614-f470d233c98e", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0041220753178"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1298324"], "spl_set_id": ["bcc41783-9213-4a8e-b7db-75b4da08551d"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["H E B"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (37808-733-20)  / 20 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC", "package_ndc": "37808-733-20", "marketing_start_date": "20230228"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (37808-733-40)  / 40 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC", "package_ndc": "37808-733-40", "marketing_start_date": "20230228"}], "brand_name": "Mucus Relief DM", "product_id": "37808-733_d2aca5b5-2bb6-41b5-a614-f470d233c98e", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]", "Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]"], "product_ndc": "37808-733", "generic_name": "Guaifenesin, Dextromethorphan HBr", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief DM", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "30 mg/1"}, {"name": "GUAIFENESIN", "strength": "600 mg/1"}], "application_number": "ANDA209692", "marketing_category": "ANDA", "marketing_start_date": "20230228", "listing_expiration_date": "20261231"}