Package 37808-427-69

{"route": ["ORAL"], "spl_id": "58f339ff-cf7c-4d4d-9437-07ec3e2818d5", "openfda": {"unii": ["7AJO3BO7QN", "Y9DL7QPE6B"], "rxcui": ["1117562"], "spl_set_id": ["0504f63e-e89c-49ad-9094-65fac328482e"], "manufacturer_name": ["HEB"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (37808-427-69)", "package_ndc": "37808-427-69", "marketing_start_date": "20180201"}], "brand_name": "Loratadine and Pseudoephedrine Sulfate", "product_id": "37808-427_58f339ff-cf7c-4d4d-9437-07ec3e2818d5", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "37808-427", "generic_name": "loratadine and pseudoephedrine sulfate", "labeler_name": "HEB", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loratadine and Pseudoephedrine Sulfate", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}, {"name": "PSEUDOEPHEDRINE SULFATE", "strength": "240 mg/1"}], "application_number": "ANDA076557", "marketing_category": "ANDA", "marketing_start_date": "20180201", "listing_expiration_date": "20261231"}