Package 68788-8782-9

{"route": ["ORAL"], "spl_id": "c45d0905-3478-4da4-b114-9f4cfb4a58ef", "openfda": {"unii": ["9044SC542W"], "rxcui": ["616402"], "spl_set_id": ["ae381859-be09-43e1-8b56-d0d8f4b49020"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8782-3)", "package_ndc": "68788-8782-3", "marketing_start_date": "20241211"}, {"sample": false, "description": "60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8782-6)", "package_ndc": "68788-8782-6", "marketing_start_date": "20241211"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8782-9)", "package_ndc": "68788-8782-9", "marketing_start_date": "20241211"}], "brand_name": "Duloxetine", "product_id": "68788-8782_c45d0905-3478-4da4-b114-9f4cfb4a58ef", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68788-8782", "generic_name": "Duloxetine", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA090694", "marketing_category": "ANDA", "marketing_start_date": "20241211", "listing_expiration_date": "20271231"}