Package 71335-2146-3

{"route": ["ORAL"], "spl_id": "20858b72-0778-46d6-be98-37d913c425b0", "openfda": {"unii": ["75046A1XTN"], "rxcui": ["861132"], "spl_set_id": ["98fa10c2-7c12-44aa-9112-e2fd6fa71d06"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-1)", "package_ndc": "71335-2146-1", "marketing_start_date": "20240403"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-2)", "package_ndc": "71335-2146-2", "marketing_start_date": "20240403"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-3)", "package_ndc": "71335-2146-3", "marketing_start_date": "20230130"}, {"sample": false, "description": "120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-4)", "package_ndc": "71335-2146-4", "marketing_start_date": "20240403"}, {"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-5)", "package_ndc": "71335-2146-5", "marketing_start_date": "20240403"}], "brand_name": "Alfuzosin Hydrochloride", "product_id": "71335-2146_20858b72-0778-46d6-be98-37d913c425b0", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "71335-2146", "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": "ANDA079057", "marketing_category": "ANDA", "marketing_start_date": "20111122", "listing_expiration_date": "20261231"}