Package 30142-739-68

{"route": ["ORAL"], "spl_id": "bf768c72-b010-4998-a3db-ac49f31294f7", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ", "6V9V2RYJ8N"], "rxcui": ["1305603"], "spl_set_id": ["5065f07d-2130-4c84-a64a-dc27ef9cb92e"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Kroger Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (30142-739-68)  / 18 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "30142-739-68", "marketing_start_date": "20251104"}], "brand_name": "mucus d", "product_id": "30142-739_bf768c72-b010-4998-a3db-ac49f31294f7", "dosage_form": "TABLET, MULTILAYER, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "30142-739", "generic_name": "guaifenesin and pseudoephedrine hydrochloride", "labeler_name": "Kroger Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "mucus d", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "600 mg/1"}, {"name": "PSEUDOEPHEDRINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA214407", "marketing_category": "ANDA", "marketing_start_date": "20251104", "listing_expiration_date": "20261231"}