Package 63629-9155-4

{"route": ["ORAL"], "spl_id": "f10b905b-346c-493f-ad51-54c0b9e0d3a4", "openfda": {"unii": ["75046A1XTN"], "rxcui": ["861132"], "spl_set_id": ["c01d4d6b-e030-4b8f-aaa9-4df0f3f8fbda"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63629-9155-1)", "package_ndc": "63629-9155-1", "marketing_start_date": "20220429"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63629-9155-2)", "package_ndc": "63629-9155-2", "marketing_start_date": "20220429"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63629-9155-3)", "package_ndc": "63629-9155-3", "marketing_start_date": "20220429"}, {"sample": false, "description": "120 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63629-9155-4)", "package_ndc": "63629-9155-4", "marketing_start_date": "20220429"}], "brand_name": "Alfuzosin hydrochloride", "product_id": "63629-9155_f10b905b-346c-493f-ad51-54c0b9e0d3a4", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "63629-9155", "generic_name": "Alfuzosin hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alfuzosin hydrochloride", "active_ingredients": [{"name": "ALFUZOSIN HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA203192", "marketing_category": "ANDA", "marketing_start_date": "20160315", "listing_expiration_date": "20261231"}