Package 0904-5833-15

{"route": ["ORAL"], "spl_id": "3e4ab498-9f9e-bd3b-e063-6294a90a9b9c", "openfda": {"unii": ["7AJO3BO7QN", "Y9DL7QPE6B"], "rxcui": ["1117562"], "spl_set_id": ["2620a150-4a2c-4fa2-a0e4-6aafe9e496c3"], "manufacturer_name": ["Major Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0904-5833-15)", "package_ndc": "0904-5833-15", "marketing_start_date": "20041117"}, {"sample": false, "description": "15 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0904-5833-48)", "package_ndc": "0904-5833-48", "marketing_start_date": "20041117"}], "brand_name": "Loratadine and Pseudoephedrine Sulfate", "product_id": "0904-5833_3e4ab498-9f9e-bd3b-e063-6294a90a9b9c", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "0904-5833", "generic_name": "Loratadine and Pseudoephedrine Sulfate", "labeler_name": "Major Pharmaceuticals", "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"}