Package 76282-302-12

{"route": ["ORAL"], "spl_id": "663c0846-dc2c-409f-9fe0-bf2901ff92da", "openfda": {"upc": ["0376282302102", "0376282302010", "0376282302126"], "unii": ["75046A1XTN"], "rxcui": ["861132"], "spl_set_id": ["f075a897-7bef-4799-b7e2-7e051c461443"], "manufacturer_name": ["Exelan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (76282-302-01)", "package_ndc": "76282-302-01", "marketing_start_date": "20121002"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (76282-302-05)", "package_ndc": "76282-302-05", "marketing_start_date": "20121002"}, {"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (76282-302-10)", "package_ndc": "76282-302-10", "marketing_start_date": "20121002"}, {"sample": false, "description": "120 TABLET, EXTENDED RELEASE in 1 BOTTLE (76282-302-12)", "package_ndc": "76282-302-12", "marketing_start_date": "20221201"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (76282-302-90)", "package_ndc": "76282-302-90", "marketing_start_date": "20190101"}], "brand_name": "Alfuzosin hydrochloride", "product_id": "76282-302_663c0846-dc2c-409f-9fe0-bf2901ff92da", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "76282-302", "generic_name": "Alfuzosin hydrochloride", "labeler_name": "Exelan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alfuzosin hydrochloride", "active_ingredients": [{"name": "ALFUZOSIN HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA090284", "marketing_category": "ANDA", "marketing_start_date": "20121002", "listing_expiration_date": "20261231"}