Package 51660-724-15

{"route": ["ORAL"], "spl_id": "a0aa350d-1d73-4951-9b48-2b35a1ae55c3", "openfda": {"unii": ["7AJO3BO7QN", "Y9DL7QPE6B"], "rxcui": ["1117562"], "spl_set_id": ["556b89ef-3b51-4faa-afb4-767a5c1b6422"], "manufacturer_name": ["Ohm Laboratories Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (51660-724-04)  / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "51660-724-04", "marketing_start_date": "20041117"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (51660-724-15)  / 15 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "51660-724-15", "marketing_start_date": "20041117"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (51660-724-56)  / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "51660-724-56", "marketing_start_date": "20041117"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (51660-724-69)  / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "51660-724-69", "marketing_start_date": "20041117"}], "brand_name": "Loratadine and Pseudoephedrine", "product_id": "51660-724_a0aa350d-1d73-4951-9b48-2b35a1ae55c3", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "51660-724", "generic_name": "loratadine and pseudoephedrine", "labeler_name": "Ohm Laboratories Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loratadine and Pseudoephedrine", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}, {"name": "PSEUDOEPHEDRINE SULFATE", "strength": "240 mg/1"}], "application_number": "ANDA076557", "marketing_category": "ANDA", "marketing_start_date": "20041117", "listing_expiration_date": "20261231"}