Package 0280-0089-02

{"route": ["ORAL"], "spl_id": "4526573a-7900-980c-e063-6394a90a5fbd", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0016500598923"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["2598125"], "spl_set_id": ["a32e2a5e-9aa0-4e7c-e053-2995a90a3190"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Bayer Healthcare LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 POUCH in 1 CARTON (0280-0089-01)  / 2 TABLET, EFFERVESCENT in 1 POUCH", "package_ndc": "0280-0089-01", "marketing_start_date": "20220405"}, {"sample": false, "description": "12 POUCH in 1 CARTON (0280-0089-02)  / 2 TABLET, EFFERVESCENT in 1 POUCH", "package_ndc": "0280-0089-02", "marketing_start_date": "20230308"}], "brand_name": "Alka Seltzer Plus Maximum Strength Cough Chest Congestion PowerFast Fizz", "product_id": "0280-0089_4526573a-7900-980c-e063-6394a90a5fbd", "dosage_form": "TABLET, EFFERVESCENT", "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": "0280-0089", "generic_name": "dextromethorphan hydrobromide, guaifenesin", "labeler_name": "Bayer Healthcare LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Alka Seltzer Plus Maximum Strength Cough Chest Congestion PowerFast Fizz", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "10 mg/1"}, {"name": "GUAIFENESIN", "strength": "200 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220405", "listing_expiration_date": "20261231"}