Package 70518-0417-1

{"route": ["ORAL"], "spl_id": "47f5ad6d-58ed-e28f-e063-6394a90a12cd", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["310385"], "spl_set_id": ["20516384-6517-48be-bd6e-718250878a76"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-0417-1)", "package_ndc": "70518-0417-1", "marketing_start_date": "20170414"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE, PLASTIC (70518-0417-2)", "package_ndc": "70518-0417-2", "marketing_start_date": "20170420"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (70518-0417-3)", "package_ndc": "70518-0417-3", "marketing_start_date": "20170426"}], "brand_name": "Fluoxetine", "product_id": "70518-0417_47f5ad6d-58ed-e28f-e063-6394a90a12cd", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70518-0417", "generic_name": "Fluoxetine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA078619", "marketing_category": "ANDA", "marketing_start_date": "20170410", "listing_expiration_date": "20271231"}