Package 65862-709-99

{"route": ["ORAL"], "spl_id": "161df518-c043-4476-968b-d0268ae03fd5", "openfda": {"upc": ["0365862709301"], "unii": ["4F86W47BR6"], "rxcui": ["1490065"], "spl_set_id": ["e8b6cbe0-c1f4-4678-b852-f629a7f6a1b5"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (65862-709-01)", "package_ndc": "65862-709-01", "marketing_start_date": "20150828"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (65862-709-03)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-709-10)", "package_ndc": "65862-709-03", "marketing_start_date": "20150828"}, {"sample": false, "description": "2000 TABLET, FILM COATED in 1 BOTTLE (65862-709-22)", "package_ndc": "65862-709-22", "marketing_start_date": "20150828"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (65862-709-30)", "package_ndc": "65862-709-30", "marketing_start_date": "20150828"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (65862-709-99)", "package_ndc": "65862-709-99", "marketing_start_date": "20150828"}], "brand_name": "Raloxifene Hydrochloride", "product_id": "65862-709_161df518-c043-4476-968b-d0268ae03fd5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Estrogen Agonist/Antagonist [EPC]", "Selective Estrogen Receptor Modulators [MoA]"], "product_ndc": "65862-709", "generic_name": "Raloxifene Hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Raloxifene Hydrochloride", "active_ingredients": [{"name": "RALOXIFENE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA204310", "marketing_category": "ANDA", "marketing_start_date": "20150828", "listing_expiration_date": "20261231"}