Package 65162-057-03

{"route": ["ORAL"], "spl_id": "767be874-7e9d-4d7d-9dc0-ba3fc6fe77d8", "openfda": {"unii": ["4F86W47BR6"], "rxcui": ["1490065"], "spl_set_id": ["3798c70b-a4b0-4811-9788-e4c9cff47ebe"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (65162-057-03)", "package_ndc": "65162-057-03", "marketing_start_date": "20160120"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (65162-057-09)", "package_ndc": "65162-057-09", "marketing_start_date": "20160120"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (65162-057-10)", "package_ndc": "65162-057-10", "marketing_start_date": "20160120"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (65162-057-11)", "package_ndc": "65162-057-11", "marketing_start_date": "20160120"}, {"sample": false, "description": "2000 TABLET, FILM COATED in 1 BOTTLE (65162-057-33)", "package_ndc": "65162-057-33", "marketing_start_date": "20160120"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (65162-057-50)", "package_ndc": "65162-057-50", "marketing_start_date": "20160120"}], "brand_name": "Raloxifene Hydrochloride", "product_id": "65162-057_767be874-7e9d-4d7d-9dc0-ba3fc6fe77d8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Estrogen Agonist/Antagonist [EPC]", "Selective Estrogen Receptor Modulators [MoA]"], "product_ndc": "65162-057", "generic_name": "Raloxifene Hydrochloride", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Raloxifene Hydrochloride", "active_ingredients": [{"name": "RALOXIFENE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA208206", "marketing_category": "ANDA", "marketing_start_date": "20160120", "listing_expiration_date": "20261231"}