Package 47335-956-08

{"route": ["ORAL"], "spl_id": "70258299-7c72-4a10-8d0c-4a5e3b2a0fc8", "openfda": {"upc": ["0347335956818"], "unii": ["75046A1XTN"], "rxcui": ["861132"], "spl_set_id": ["d2af616e-673a-4fdd-ace8-db2d0f154604"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-08)", "package_ndc": "47335-956-08", "marketing_start_date": "20111122"}, {"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-18)", "package_ndc": "47335-956-18", "marketing_start_date": "20111122"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-81)", "package_ndc": "47335-956-81", "marketing_start_date": "20111122"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-83)", "package_ndc": "47335-956-83", "marketing_start_date": "20111122"}, {"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-88)", "package_ndc": "47335-956-88", "marketing_start_date": "20111122"}], "brand_name": "Alfuzosin Hydrochloride", "product_id": "47335-956_70258299-7c72-4a10-8d0c-4a5e3b2a0fc8", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "47335-956", "generic_name": "Alfuzosin Hydrochloride", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "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"}