Package 68788-4025-3

{"route": ["ORAL"], "spl_id": "c5aac428-d929-4688-a9d5-4e9314aa62cc", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596930", "596934"], "spl_set_id": ["c5aac428-d929-4688-a9d5-4e9314aa62cc"], "manufacturer_name": ["Preferred Phamaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-4025-3)", "package_ndc": "68788-4025-3", "marketing_start_date": "20250915"}, {"sample": false, "description": "60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-4025-6)", "package_ndc": "68788-4025-6", "marketing_start_date": "20250915"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-4025-9)", "package_ndc": "68788-4025-9", "marketing_start_date": "20250915"}], "brand_name": "Duloxetine", "product_id": "68788-4025_c5aac428-d929-4688-a9d5-4e9314aa62cc", "dosage_form": "CAPSULE, DELAYED RELEASE PELLETS", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68788-4025", "generic_name": "Duloxetine", "labeler_name": "Preferred Phamaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA090776", "marketing_category": "ANDA", "marketing_start_date": "20250915", "listing_expiration_date": "20261231"}