Package 47335-587-18

{"route": ["ORAL"], "spl_id": "95e952a3-5a7d-4b4c-9ac8-b5256a4371c3", "openfda": {"upc": ["0347335586831"], "unii": ["UZX80K71OE"], "rxcui": ["485440", "485442", "485465"], "spl_set_id": ["8bb1965e-7845-4c5b-b021-38e251303d68"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (47335-587-08)", "package_ndc": "47335-587-08", "marketing_start_date": "20140415"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (47335-587-18)", "package_ndc": "47335-587-18", "marketing_start_date": "20140415"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (47335-587-83)", "package_ndc": "47335-587-83", "marketing_start_date": "20140415"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (47335-587-88)", "package_ndc": "47335-587-88", "marketing_start_date": "20140415"}], "brand_name": "ESZOPICLONE", "product_id": "47335-587_95e952a3-5a7d-4b4c-9ac8-b5256a4371c3", "dosage_form": "TABLET, FILM COATED", "product_ndc": "47335-587", "dea_schedule": "CIV", "generic_name": "ESZOPICLONE", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ESZOPICLONE", "active_ingredients": [{"name": "ESZOPICLONE", "strength": "2 mg/1"}], "application_number": "ANDA091103", "marketing_category": "ANDA", "marketing_start_date": "20140415", "listing_expiration_date": "20261231"}