Package 55910-529-08

{"route": ["ORAL"], "spl_id": "850efbf9-ed31-45de-986b-bd69fb6de654", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0050844527089"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["b65baa7c-8197-4361-b3ef-e60eba38dca1"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["DOLGENCORP, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (55910-529-08)  / 12 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "55910-529-08", "marketing_start_date": "20050806"}], "brand_name": "Sinus Severe Daytime", "product_id": "55910-529_850efbf9-ed31-45de-986b-bd69fb6de654", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "55910-529", "generic_name": "Acetaminophen, Guaifenesin, Phenylephrine HCl", "labeler_name": "DOLGENCORP, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sinus Severe", "brand_name_suffix": "Daytime", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 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": "20050806", "listing_expiration_date": "20261231"}