Package 65862-249-05

{"route": ["ORAL"], "spl_id": "d8c832c1-9455-4647-822a-ee4f35ba0560", "openfda": {"upc": ["0365862249302"], "unii": ["75046A1XTN"], "rxcui": ["861132"], "spl_set_id": ["d163369b-e44b-4591-b166-7ddd0c1c13c0"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-249-01)", "package_ndc": "65862-249-01", "marketing_start_date": "20120830"}, {"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-249-05)", "package_ndc": "65862-249-05", "marketing_start_date": "20120830"}, {"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-249-30)", "package_ndc": "65862-249-30", "marketing_start_date": "20120830"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-249-90)", "package_ndc": "65862-249-90", "marketing_start_date": "20120830"}, {"sample": false, "description": "1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-249-99)", "package_ndc": "65862-249-99", "marketing_start_date": "20120830"}], "brand_name": "Alfuzosin Hydrochloride", "product_id": "65862-249_d8c832c1-9455-4647-822a-ee4f35ba0560", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "65862-249", "generic_name": "Alfuzosin Hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alfuzosin Hydrochloride", "active_ingredients": [{"name": "ALFUZOSIN HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA079060", "marketing_category": "ANDA", "marketing_start_date": "20120830", "listing_expiration_date": "20261231"}