Package 21130-724-69

{"route": ["ORAL"], "spl_id": "92f68316-fe4c-4e9f-8f18-cbb66ac6deae", "openfda": {"unii": ["7AJO3BO7QN", "Y9DL7QPE6B"], "rxcui": ["1117562"], "spl_set_id": ["c1e1e0ca-30df-4ace-a7b6-c66a3c5ab676"], "manufacturer_name": ["Safeway Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (21130-724-15)", "package_ndc": "21130-724-15", "marketing_start_date": "20041117"}, {"sample": false, "description": "10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (21130-724-69)", "package_ndc": "21130-724-69", "marketing_start_date": "20041117"}], "brand_name": "Loratadine and Pseudoephedrine Sulfate", "product_id": "21130-724_92f68316-fe4c-4e9f-8f18-cbb66ac6deae", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "21130-724", "generic_name": "Loratadine and Pseudoephedrine Sulfate", "labeler_name": "Safeway Inc.", "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": "20041117", "listing_expiration_date": "20261231"}