Package 80425-0441-1

{"route": ["ORAL"], "spl_id": "25137bab-44cd-121d-e063-6394a90a2717", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596930", "596934"], "spl_set_id": ["19afed24-39ad-daf1-e063-6394a90ad737"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0441-1)", "package_ndc": "80425-0441-1", "marketing_start_date": "20241022"}, {"sample": false, "description": "60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0441-2)", "package_ndc": "80425-0441-2", "marketing_start_date": "20241022"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0441-3)", "package_ndc": "80425-0441-3", "marketing_start_date": "20241022"}], "brand_name": "Duloxetine", "product_id": "80425-0441_25137bab-44cd-121d-e063-6394a90a2717", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "80425-0441", "generic_name": "Duloxetine", "labeler_name": "Advanced Rx of Tennessee, LLC", "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": "20241022", "listing_expiration_date": "20261231"}