Package 0615-8495-05

{"route": ["ORAL"], "spl_id": "3ae078dc-e9a7-441a-b0c2-6ecdbb120a9d", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596926", "596930", "596934"], "spl_set_id": ["54749431-430e-4532-97f7-4b1cd8dd252e"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "15 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (0615-8495-05)", "package_ndc": "0615-8495-05", "marketing_start_date": "20240103"}, {"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (0615-8495-39)", "package_ndc": "0615-8495-39", "marketing_start_date": "20240103"}], "brand_name": "Duloxetine", "product_id": "0615-8495_3ae078dc-e9a7-441a-b0c2-6ecdbb120a9d", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "0615-8495", "generic_name": "Duloxetine", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA090694", "marketing_category": "ANDA", "marketing_start_date": "20131211", "listing_expiration_date": "20261231"}