Package 70518-1011-2

{"route": ["ORAL"], "spl_id": "4849b7fd-a904-8fde-e063-6394a90a1f0f", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596934"], "spl_set_id": ["ba4adb77-45be-4310-a877-766692f22e5e"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-1011-0)", "package_ndc": "70518-1011-0", "marketing_start_date": "20180212"}, {"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1011-1)", "package_ndc": "70518-1011-1", "marketing_start_date": "20190417"}, {"sample": false, "description": "60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1011-2)", "package_ndc": "70518-1011-2", "marketing_start_date": "20200504"}], "brand_name": "Duloxetine", "product_id": "70518-1011_4849b7fd-a904-8fde-e063-6394a90a1f0f", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "70518-1011", "generic_name": "Duloxetine", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA208706", "marketing_category": "ANDA", "marketing_start_date": "20180212", "listing_expiration_date": "20271231"}