Package 0280-0061-01

{"route": ["ORAL"], "spl_id": "45262b77-58b2-6e5f-e063-6394a90a443c", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0016500584209"], "unii": ["362O9ITL9D", "9D2RTI9KYH", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1656815"], "spl_set_id": ["a6a2dd4a-a3c8-2dfa-e053-2995a90ada86"], "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": "2 BLISTER PACK in 1 CARTON (0280-0061-01)  / 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "0280-0061-01", "marketing_start_date": "20200601"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (0280-0061-02)  / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "0280-0061-02", "marketing_start_date": "20200601"}], "brand_name": "Alka-Seltzer Plus Maximum Strength Cough, Mucus and Congestion Powermax", "product_id": "0280-0061_45262b77-58b2-6e5f-e063-6394a90a443c", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "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]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "0280-0061", "generic_name": "acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride", "labeler_name": "Bayer HealthCare LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Alka-Seltzer Plus Maximum Strength Cough, Mucus and Congestion Powermax", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "10 mg/1"}, {"name": "GUAIFENESIN", "strength": "200 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200601", "listing_expiration_date": "20261231"}