Package 71209-082-11

{"route": ["ORAL"], "spl_id": "14d4c334-b49d-4479-a91e-20b7276b4eca", "openfda": {"upc": ["0371209082112"], "unii": ["4F86W47BR6"], "rxcui": ["1490065"], "spl_set_id": ["a46bcc4f-f63d-4200-836d-a653a3c616db"], "manufacturer_name": ["Cadila Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (71209-082-01)", "package_ndc": "71209-082-01", "marketing_start_date": "20171230"}, {"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (71209-082-05)", "package_ndc": "71209-082-05", "marketing_start_date": "20171230"}, {"sample": false, "description": "1000 TABLET, COATED in 1 BOTTLE (71209-082-11)", "package_ndc": "71209-082-11", "marketing_start_date": "20211213"}, {"sample": false, "description": "2000 TABLET, COATED in 1 BOTTLE (71209-082-13)", "package_ndc": "71209-082-13", "marketing_start_date": "20171230"}], "brand_name": "Raloxifene hydrochloride", "product_id": "71209-082_14d4c334-b49d-4479-a91e-20b7276b4eca", "dosage_form": "TABLET, COATED", "pharm_class": ["Estrogen Agonist/Antagonist [EPC]", "Selective Estrogen Receptor Modulators [MoA]"], "product_ndc": "71209-082", "generic_name": "Raloxifene hydrochloride", "labeler_name": "Cadila Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Raloxifene hydrochloride", "active_ingredients": [{"name": "RALOXIFENE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA211324", "marketing_category": "ANDA", "marketing_start_date": "20171230", "listing_expiration_date": "20261231"}